FDA Device Intelligence
Home › PRINCETON BIOMEDITECH CORPORATION › Status BTA Card

Status BTA Card

PRINCETON BIOMEDITECH CORPORATION · Model BSP-307-10-00 · UDI-DI 10743816001409

MMW
1
510(k) clearances
6
Adverse events
1
Recalls
5
Facilities

Description

Status BTA (CLIA Waived); 10 Test Kit

Recalls

DateFirmReason
2004-02-19VysisSome of the control slides did not have adequate cells deposited upon their surface.

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 docs
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.