SERIES 40 & SERIES 42 CRYOPROBES (R SERIES)— 510(k) K882962

Substantially Equivalent

Spembly Medical , Ltd.

FDA 510(k) clearance K882962 for SERIES 40 & SERIES 42 CRYOPROBES (R SERIES), Substantially Equivalent on 1988-08-08. Applicant: Spembly Medical , Ltd..

Clearance details

Applicant: Spembly Medical , Ltd.
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 1988-07-14
Decision date: 1988-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.