AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS— 510(k) K802159

Name: FDA 510(k) clearance K802159
Creator: U.S. Food and Drug Administration
Published: 1980-10-10

Substantially Equivalent

Panmed, Inc.

FDA 510(k) clearance K802159 for AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS, Substantially Equivalent on 1980-10-10. Applicant: Panmed, Inc.. Device class: 1.

Clearance details

Applicant: Panmed, Inc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1980-09-08
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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