KERATINOCYTE GROWTH MEDIUM (KGM)— 510(k) K881000

Name: FDA 510(k) clearance K881000
Creator: U.S. Food and Drug Administration
Published: 1988-03-21

Substantially Equivalent

Clonetics Corp.

FDA 510(k) clearance K881000 for KERATINOCYTE GROWTH MEDIUM (KGM), Substantially Equivalent on 1988-03-21. Applicant: Clonetics Corp.. Device class: 1.

Clearance details

Applicant: Clonetics Corp.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1988-03-08
Decision date: 1988-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIT

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K892938 — AMNIO-GROW TM1989-05-22
K890700 — MELANOCYTE GROWTH MEDIUM (MGM)1989-02-24
K890701 — ENDOTHELIAL GROWTH MEDIUM (EGM)1989-02-24
K890482 — ABC, ABC-1X, ABC(TM)1989-02-10
K884654 — ALPHACALF SERUM1988-11-30

More clearances from Clonetics Corp.

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K880999 — EPIPACK1988-03-24

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