ANTI-CONVULSANT DRUG CONTROL— 510(k) K770975

Name: FDA 510(k) clearance K770975
Creator: U.S. Food and Drug Administration
Published: 1977-06-08

Substantially Equivalent

Lederle Laboratories

FDA 510(k) clearance K770975 for ANTI-CONVULSANT DRUG CONTROL, Substantially Equivalent on 1977-06-08. Applicant: Lederle Laboratories. Device class: 2.

Clearance details

Applicant: Lederle Laboratories
Product code: Code DIC
Device class: Class 2
Regulation: 21 CFR 862.3040
Advisory panel: Clinical Toxicology
Date received: 1977-05-31
Decision date: 1977-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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