ULTRASOUND PROCEDURE TRAY AMNICENTESIS TRAY— 510(k) K890463

Name: FDA 510(k) clearance K890463
Creator: U.S. Food and Drug Administration
Published: 1989-04-07

Unknown

Critical Specialties, Inc.

FDA 510(k) clearance K890463 for ULTRASOUND PROCEDURE TRAY AMNICENTESIS TRAY, Unknown on 1989-04-07. Applicant: Critical Specialties, Inc.. Device class: 1.

Clearance details

Applicant: Critical Specialties, Inc.
Product code: Code HIO
Device class: Class 1
Regulation: 21 CFR 884.1550
Advisory panel: Obstetrics/Gynecology
Date received: 1989-01-30
Decision date: 1989-04-07
Decision: Unknown
Clearance type: Traditional
Location: West Chester, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIO

view all

K960203 — G.E. STERILE AMNIOCENTESIS TRAY1996-03-14
K955679 — RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAY1996-03-12
K914419 — AMNIOTEST(TM)1993-09-01
K922960 — VARIOUS CAMEO MED AMNIOCENTESIS TRAYS, DISPOSABLE1992-11-05
K921738 — SONO-VU US(TM), MODIFICATION1992-04-27

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