CARDIOSCAN - TM BEING APPLIED FOR— 510(k) K841263

Name: FDA 510(k) clearance K841263
Creator: U.S. Food and Drug Administration
Published: 1984-10-19

Substantially Equivalent

Interspec, Inc.

FDA 510(k) clearance K841263 for CARDIOSCAN - TM BEING APPLIED FOR, Substantially Equivalent on 1984-10-19. Applicant: Interspec, Inc.. Device class: 2.

Clearance details

Applicant: Interspec, Inc.
Product code: Code DXK
Device class: Class 2
Regulation: 21 CFR 870.2330
Advisory panel: Cardiovascular
Date received: 1984-03-26
Decision date: 1984-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Conshohocken, PA, US

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