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Accessory box AB03
PATH medical GmbH · Model 100261-BL · UDI-DI 04260223143380
GWJ
Prescription
10
510(k) clearances
119
Adverse events
4
Recalls
58
Facilities
Description
Accessory Set with Bio-Logic Branding including: 4pcs. 100013 Probe Tip PT-A 4pcs. 100014-W Probe Tip PT-S 1pc. 100129 Test Cavity PT-A 1pc. 100160 Test Cavity PT-S 10pcs. 100063 Ear Tip ET-03 10pcs. 100064 Ear Tip ET-10 7pcs 100125 Ear Tip ET-11 5pcs. 100839 Ear Tip Soft ET-17 6pcs. 100838 Ear Tip Soft ET-16 10pcs. 100144 Ear Tip ET-13 4pcs. 100230 Ear Tip Soft ET-14 10pcs. 100030 Ear Tip ET-S02 10pcs. 100031 Ear Tip ET-S03 10pcs. 100032 Ear Tip ET-S10 10pcs. 100840 Ear Tip Soft ET-S11 1pc. 100151 Cleaning Tool CT-01
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-06 | PATH | Following a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude acceptance |
| 2019-05-28 | GN Otometrics | There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock. |
| 2010-06-04 | Natus Medical Inc | There is insufficient evidence to support any claims for safety and efficacy on the SonaMed Clarity devices. |
| 2008-10-21 | Intelligent Hearing Systems Corp. | This was a marketing correction mandated by the United States Food and Drug Administration (USFDA). USFDA notified Intelligent Hearing Systems that 501(k) premarket notification ap |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
