AUTOCUFF (PHOTOS ENCLOSED WITH 510K— 510(k) K822286

Substantially Equivalent

Partamed, Inc.

FDA 510(k) clearance K822286 for AUTOCUFF (PHOTOS ENCLOSED WITH 510K, Substantially Equivalent on 1982-08-27. Applicant: Partamed, Inc..

Clearance details

Applicant: Partamed, Inc.
Product code: Code KZD
Advisory panel: General Hospital
Date received: 1982-07-30
Decision date: 1982-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KZD

product code KZD

Death: 4
Total: 4

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.