MODIFIED HUMAN TUBAL FLUID (MHTF) WITH/WITHOUT PENICILLIN G DOLIUM, WITH/WITHOUT STREPTOMYCIN SULFATE— 510(k) K951835

Name: FDA 510(k) clearance K951835
Creator: U.S. Food and Drug Administration
Published: 1995-08-11

Substantially Equivalent

Life Technologies, Inc.

FDA 510(k) clearance K951835 for MODIFIED HUMAN TUBAL FLUID (MHTF) WITH/WITHOUT PENICILLIN G DOLIUM, WITH/WITHOUT STREPTOMYCIN SULFATE, Substantially Equivalent on 1995-08-11. Applicant: Life Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Life Technologies, Inc.
Product code: Code MFD
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1995-04-20
Decision date: 1995-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Island, NY, US

Download summary PDF View on FDA.gov ↗

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