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QBC Diagnostics

DRUCKER DIAGNOSTICS · Model 427421 · UDI-DI 00858092006222

JSYGKZ
5
510(k) clearances
4
Adverse events
1
Recalls
7
Facilities

Description

QBC F.A.S.T. AFB Detection System - ParaLens Advance with 20X & 40X Objectives and Centrifuge (230V)

Recalls

DateFirmReason
2009-05-06Remel, IncThe plate labeling is incorrect, but the outer box labeling is correct

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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.