CELLSOFT(TM)-CASA (SERIES 1000,2000 & 3000)— 510(k) K872145

Name: FDA 510(k) clearance K872145
Creator: U.S. Food and Drug Administration
Published: 1987-11-13

Substantially Equivalent

Cryo Corp.

FDA 510(k) clearance K872145 for CELLSOFT(TM)-CASA (SERIES 1000,2000 & 3000), Substantially Equivalent on 1987-11-13. Applicant: Cryo Corp.. Device class: 2.

Clearance details

Applicant: Cryo Corp.
Product code: Code GKL
Device class: Class 2
Regulation: 21 CFR 864.5200
Advisory panel: Hematology
Date received: 1987-06-04
Decision date: 1987-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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