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INSTRUMENT SPECIALISTS, INC. · Model Foam Pad - K Table · UDI-DI 00810045920528
10
510(k) clearances
28
Adverse events
1
Recalls
51
Facilities
Description
2" Contoured Foam Pad - K Table
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-05-15 | Stryker Medical Div. of Stryker Corporation | An incorrect pin may have been used during assembly and therefore the device may give way during use. |
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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.