PULSE CUFF RECORDER MODEL PCR100— 510(k) K863702

Name: FDA 510(k) clearance K863702
Creator: U.S. Food and Drug Administration
Published: 1987-06-12

Substantially Equivalent

Imex Medical Systems, Inc.

FDA 510(k) clearance K863702 for PULSE CUFF RECORDER MODEL PCR100, Substantially Equivalent on 1987-06-12. Applicant: Imex Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Imex Medical Systems, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1986-09-23
Decision date: 1987-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Golden, CO, US

Download summary PDF View on FDA.gov ↗

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