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Keeler Disposable Tonomate - BX 100
KEELER LIMITED · Model 2414-P-7039 · UDI-DI 05055272718042
10
510(k) clearances
11
Adverse events
2
Recalls
64
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a |
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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.