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Marketlab Inc

MARKETLAB INC. · Model 5681 · UDI-DI 00817517020526

KSS
6
510(k) clearances
72
Adverse events
0
Recalls
39
Facilities

Description

Hematype Segment Device-100/pk.

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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.