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Sklar®

SKLAR CORPORATION · Model 10-1738 · UDI-DI 10649111375019

FSM
10
510(k) clearances
2,280
Adverse events (2 deaths)
0
Recalls
875
Facilities

Description

INSTR/CATH TRAY 8 7/8"X 5"X 2"

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.