INORGANIC PHOSPHORUS REAGENT— 510(k) K955937

Name: FDA 510(k) clearance K955937
Creator: U.S. Food and Drug Administration
Published: 1996-03-12

Substantially Equivalent

Derma Media Lab., Inc.

FDA 510(k) clearance K955937 for INORGANIC PHOSPHORUS REAGENT, Substantially Equivalent on 1996-03-12. Applicant: Derma Media Lab., Inc.. Device class: 1.

Clearance details

Applicant: Derma Media Lab., Inc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1995-12-21
Decision date: 1996-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Fe Springs, CA, US

Download summary PDF View on FDA.gov ↗

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