SWIVEL ADAPTER— 510(k) K900642

Name: FDA 510(k) clearance K900642
Creator: U.S. Food and Drug Administration
Published: 1990-03-19

Substantially Equivalent

Williams Specialty Products, Inc.

FDA 510(k) clearance K900642 for SWIVEL ADAPTER, Substantially Equivalent on 1990-03-19. Applicant: Williams Specialty Products, Inc.. Device class: 2.

Clearance details

Applicant: Williams Specialty Products, Inc.
Product code: Code HHI
Device class: Class 2
Regulation: 21 CFR 884.5070
Advisory panel: Obstetrics/Gynecology
Date received: 1990-02-09
Decision date: 1990-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Encino, CA, US

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