FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODIFIED STICK-GARD SAFETY NEEDLE

K Number: K902196 · Decision Jun 26, 1990
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
16
Review Days
41

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MODIFIED STICK-GARD SAFETY NEEDLE
K Number
K902196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ziehm International, Inc.
Date Received
May 16, 1990
Decision Date
June 26, 1990
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FPA Set, Administration, Intravascular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FPA), ordered by most recent decision date.

View all

Other Clearances by Ziehm International, Inc.

K Number Device Name
K011292 ZIEHM VISION
K910455 IMS DISPOSABLE HOLDER WITH NEEDLE RETRACTOR
K894021 MOBILE X-RAY UNIT
K894041 PUMP-JECT SYRINGE WITH LUER-LOCK
K890620 STICK-GARD SAFETY NEEDLE
K882133 MAMMO M
K843311 IV ADMIN. SET FOR MVP 1 INFUSION PUMP
K842263 MTP E.V. INFUSION PUMP
K831407 CARDIAC OUTPUT COMPUTER
K830453 IV ADMINISTRATION SETS - MVP INFUSION
Search all 16 clearances from Ziehm International, Inc. →