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Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901001 · UDI-DI 00732094084580

ETY Prescription
1
510(k) clearances
6
Adverse events
1
Recalls
14
Facilities

Description

Welch Allyn MicroTymp-2 Ear-Tip Set; Qty. 5 each of Small and Extra Large, Qty. 10 each of Medium and Large; Qty. 30

Recalls

DateFirmReason
2005-06-27Natus Medical IncInternal investigation revealed that Preamp cable assemblies in the device had not been properly tested, which could lead to potential shock to users.

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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.