PULSETAKER— 510(k) K782131

Substantially Equivalent

Van, Cott, Bagley, Cornwall & Mccarth

FDA 510(k) clearance K782131 for PULSETAKER, Substantially Equivalent on 1979-01-15. Applicant: Van, Cott, Bagley, Cornwall & Mccarth.

Clearance details

Applicant: Van, Cott, Bagley, Cornwall & Mccarth
Product code: Code DRT
Advisory panel: Cardiovascular
Date received: 1978-12-27
Decision date: 1979-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DRT

product code DRT

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.