ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880— 510(k) K982055

Substantially Equivalent

Cryomedical Sciences, Inc.

FDA 510(k) clearance K982055 for ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880, Substantially Equivalent on 1998-09-08. Applicant: Cryomedical Sciences, Inc..

Clearance details

Applicant: Cryomedical Sciences, Inc.
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 1998-06-11
Decision date: 1998-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

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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.