FORCEPS, OB, NON-COMPRESSIVE— 510(k) K771106

Name: FDA 510(k) clearance K771106
Creator: U.S. Food and Drug Administration
Published: 1977-07-01

Substantially Equivalent

Zeppelin Medizinlechnik GmbH

FDA 510(k) clearance K771106 for FORCEPS, OB, NON-COMPRESSIVE, Substantially Equivalent on 1977-07-01. Applicant: Zeppelin Medizinlechnik GmbH. Device class: 2.

Clearance details

Applicant: Zeppelin Medizinlechnik GmbH
Product code: Code HDA
Device class: Class 2
Regulation: 21 CFR 884.4400
Advisory panel: Obstetrics/Gynecology
Date received: 1977-06-20
Decision date: 1977-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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