Home › AMBLER SURGICAL CORP. › Ambler Surgical
Ambler Surgical
AMBLER SURGICAL CORP. · Model Ostium probe · UDI-DI 00190660127619
KAK
Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
93
Facilities
Description
Ostium probe, 7 1/2'', double-ended, curved, one end at 90 degrees, hexagonal handle
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-17 | Vital Signs Colorado Inc. | There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.