Home › SAKURA FINETEK U.S.A., INC. › Accu-Cut® SRM™ 200
Accu-Cut® SRM™ 200
SAKURA FINETEK U.S.A., INC. · Model 1437 · UDI-DI 00615233012944
5
510(k) clearances
56
Adverse events
1
Recalls
27
Facilities
Description
Low-Profile Back Plate (part of item 1435)
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. |
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.