FDA Device Intelligence
Home › Device types › GSK

Antiserum, Francisella Tularensis

FDA product code GSK · Class 2 · Microbiology

2
Registered devices
0
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

FRANCISELLA TULARENSIS ANTISERUM — GERMAINE LABORATORIES, INCBD Francisella Tularensis Antiserum — BECTON, DICKINSON AND COMPANY

Recent recalls

DateFirmReason
2004-10-20BD Diagnostic SystemsFebrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.

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
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.