FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

URETERAL CATHETER

K Number: K930483 · Decision Jul 16, 1993
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
27
Applicant Total
29
Review Days
168

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
URETERAL CATHETER
K Number
K930483
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Surgitek
Date Received
January 29, 1993
Decision Date
July 16, 1993
Product Code
EYB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EYB Catheter, Ureteral, Gastro-Urology

Similar 510(k) Clearances

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

View all

Other Clearances by Surgitek

K Number Device Name
K946296 QUADRA-COIL URETERAL STENT
K944391 OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM
K943491 RIGHT ANGLE UROLOGIC LASER FIBER
K941952 SURGITEK INFUSER
K933261 GRASPING FORCEPS
K933260 HELICAL STONE/FLATWIRE STONE BASKETS
K930733 URETERAL STENT
K926344 HYDROPHILIC COATED GUIDEWIRE
K920451 ENDOTEK ULTRA SYSTEM
K922542 GRASPING FORCEPS
Search all 29 clearances from Surgitek →