FDA Device Intelligence
Home › BC GROUP INTERNATIONAL, INC. › Gossen Metrawatt SECULIFE

Gossen Metrawatt SECULIFE

BC GROUP INTERNATIONAL, INC. · Model DF+ · UDI-DI 00863313000347

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

Description

Defibrillator Analyzer, with Transcutaneous Pacemaker Input - private labeled for Gossen Metrawatt

Recalls

DateFirmReason
2015-10-28BC Group International IncDevice is not functioning as intended: Two wires running to the ECG distribution circuit board are reversed resulting in inverted waveforms.

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.