ACTICLOT C KIT— 510(k) K884941

Substantially Equivalent

American Diagnostic Corp.

FDA 510(k) clearance K884941 for ACTICLOT C KIT, Substantially Equivalent on 1989-03-13. Applicant: American Diagnostic Corp.. Device class: 2.

Clearance details

Applicant: American Diagnostic Corp.
Product code: Code GGP
Device class: Class 2
Regulation: 21 CFR 864.7290
Advisory panel: Hematology
Date received: 1988-11-28
Decision date: 1989-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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