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Accu-Cut® SRM™ 200
SAKURA FINETEK U.S.A., INC. · Model 1429 · UDI-DI 08720177655170
5
510(k) clearances
56
Adverse events
1
Recalls
27
Facilities
Description
Rotary Microtome (Retracting)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-08-12 | Richard-Allan Scientific Company | The firm has received two complaints of finger lacerations in operators of this device. |
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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.