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

UMBILICAL VESSEL CATHETER

K Number: K840339 · Decision Jul 25, 1984
Classifications
1
FEI Numbers
16
Registration Numbers
17
Same Product Code
33
Applicant Total
13
Review Days
182

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
UMBILICAL VESSEL CATHETER
K Number
K840339
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Catheter Technology Corp.
Date Received
January 25, 1984
Decision Date
July 25, 1984
Product Code
FOS
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
FOS Catheter, Umbilical Artery

Similar 510(k) Clearances

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

View all

Other Clearances by Catheter Technology Corp.

K Number Device Name
K880571 CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM
K871080 PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER
K871998 GROSHONG CV CATHETER REPAIR KIT
K860256 BRAWN AND GROSHONG CATHETERS
K842577 CATH-TECH POLYURETHANE UMBILICAL VESS
K842147 CATH-TECH CHOLANGIOGRAPHY CATHETER
K831386 GROSHONG CATHETER, LONG TERM TYPE
K831366 TESTCORP PREG
K831365 TESTCORP ANA
K831361 BETA-PREG
Search all 13 clearances from Catheter Technology Corp. →