PACER MONITOR, PULSE WIDTH— 510(k) K772178

Substantially Equivalent

Survival Technology, Inc.

FDA 510(k) clearance K772178 for PACER MONITOR, PULSE WIDTH, Substantially Equivalent on 1977-12-08. Applicant: Survival Technology, Inc..

Clearance details

Applicant: Survival Technology, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1977-11-22
Decision date: 1977-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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