HEMO-O-LOK— 510(k) K941972

Substantially Equivalent

King & Spalding

FDA 510(k) clearance K941972 for HEMO-O-LOK, Substantially Equivalent on 1994-06-29. Applicant: King & Spalding.

Clearance details

Applicant: King & Spalding
Product code: Code FZP
Advisory panel: General, Plastic Surgery
Date received: 1994-04-22
Decision date: 1994-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FZP

product code FZP

Death: 11
Injury: 726
Malfunction: 10,830
Other: 1
Total: 11,568

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.