PACEVIEW— 510(k) K895535

Substantially Equivalent

Micromedical

FDA 510(k) clearance K895535 for PACEVIEW, Substantially Equivalent on 1990-03-19. Applicant: Micromedical. Device class: 2.

Clearance details

Applicant: Micromedical
Product code: Code KRE
Device class: Class 2
Regulation: 21 CFR 870.3640
Advisory panel: Cardiovascular
Date received: 1989-09-13
Decision date: 1990-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gettysburg, PA, US

Download summary PDF View on FDA.gov ↗

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K895534 — BIOLOG1990-03-19

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