RPMI 1640 W/GLUTAMINE W/HEPES— 510(k) K860282

Name: FDA 510(k) clearance K860282
Creator: U.S. Food and Drug Administration
Published: 1986-02-05

Substantially Equivalent

Newport Biosystems, Inc.

FDA 510(k) clearance K860282 for RPMI 1640 W/GLUTAMINE W/HEPES, Substantially Equivalent on 1986-02-05. Applicant: Newport Biosystems, Inc.. Device class: 1.

Clearance details

Applicant: Newport Biosystems, Inc.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1986-01-28
Decision date: 1986-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, 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.