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

RIGHT ANGLE UROLOGIC LASER FIBER

K Number: K943491 · Decision Aug 5, 1994
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
29
Review Days
17

Basic Information

Device Name
RIGHT ANGLE UROLOGIC LASER FIBER
K Number
K943491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SURGITEK
Date Received
July 19, 1994
Decision Date
August 5, 1994
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), 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
K941952 SURGITEK INFUSER
K933260 HELICAL STONE/FLATWIRE STONE BASKETS
K933261 GRASPING FORCEPS
K930733 URETERAL STENT
K930483 URETERAL CATHETER
K926344 HYDROPHILIC COATED GUIDEWIRE
K920451 ENDOTEK ULTRA SYSTEM
K922542 GRASPING FORCEPS
Search all 29 clearances from SURGITEK →