SODIUM PYRUVATE (100MM)— 510(k) K820495

Name: FDA 510(k) clearance K820495
Creator: U.S. Food and Drug Administration
Published: 1982-03-26

Substantially Equivalent

Dutchland Laboratories, Inc.

FDA 510(k) clearance K820495 for SODIUM PYRUVATE (100MM), Substantially Equivalent on 1982-03-26. Applicant: Dutchland Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Dutchland Laboratories, Inc.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1982-02-23
Decision date: 1982-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIT

view all

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 Dutchland Laboratories, Inc.

view all

K821911 — S-MEM-JOKLIK'S POWDER1982-07-27
K821912 — MCCOY'S POWDER MEDIUM 5A SUSPENSION1982-07-27
K821913 — ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM1982-07-27
K821914 — COON'S F-12 POWDER MEDIUM1982-07-27
K821915 — BME AUTOCLAVABLE MEDIUM1982-07-27

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