CANNULA, SUCTION UTERINE— 510(k) K900641

Name: FDA 510(k) clearance K900641
Creator: U.S. Food and Drug Administration
Published: 1990-03-30

Substantially Equivalent

Williams Specialty Products, Inc.

FDA 510(k) clearance K900641 for CANNULA, SUCTION UTERINE, Substantially Equivalent on 1990-03-30. 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: 1990-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Encino, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHI

view all

K171440 — Berkeley VC-10 Vacuum Curettage System2017-09-29
K030935 — BERKELEY V-10 VACUUM CURETTAGE SYSTEM2003-06-23
K983181 — CYTOPREP1998-11-16
K931205 — MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER1994-03-15
K904160 — CYTOSMEAR BRUSH1990-11-02

More clearances from Williams Specialty Products, Inc.

view all

K900642 — SWIVEL ADAPTER1990-03-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.