MIDWIFERY/OBSTETRICAL FORCEPS— 510(k) K890385

Name: FDA 510(k) clearance K890385
Creator: U.S. Food and Drug Administration
Published: 1989-03-01

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890385 for MIDWIFERY/OBSTETRICAL FORCEPS, Substantially Equivalent on 1989-03-01. Applicant: Kinetic Medical Products. Device class: 2.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code HDA
Device class: Class 2
Regulation: 21 CFR 884.4400
Advisory panel: Obstetrics/Gynecology
Date received: 1989-01-23
Decision date: 1989-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

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