CELLGRO HEPES BUFFER SOLUTION— 510(k) K860623

Substantially Equivalent

Mediatech, Inc.

FDA 510(k) clearance K860623 for CELLGRO HEPES BUFFER SOLUTION, Substantially Equivalent on 1986-03-03. Applicant: Mediatech, Inc.. Device class: 1.

Clearance details

Applicant: Mediatech, Inc.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1986-02-19
Decision date: 1986-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIT

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 Mediatech, Inc.

K854567 — PENICILLIN/STREPTOMYCIN SOLUTION1985-12-06
K852475 — CELLGRO WILLIAMS' MEDIUM E1985-07-12
K852485 — CELLGRO(ISCOVE'S MEDIUM) MODIFICATION1985-07-12
K852602 — MCCOY'S 5A MEDIUM-LIQUID FORM1985-07-12
K852603 — MCCOY'S 5A MEDIUM - POWDERED FORM1985-07-12

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