MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER— 510(k) K972823

Name: FDA 510(k) clearance K972823
Creator: U.S. Food and Drug Administration
Published: 1997-10-10

Substantially Equivalent

A & A Medical, Inc.

FDA 510(k) clearance K972823 for MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER, Substantially Equivalent on 1997-10-10. Applicant: A & A Medical, Inc.. Device class: 2.

Clearance details

Applicant: A & A Medical, Inc.
Product code: Code MFD
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1997-07-30
Decision date: 1997-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

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