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

HYDROPHILIC COATED GUIDEWIRE

K Number: K926344 · Decision Mar 5, 1993
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
29
Review Days
78

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Basic Information

Device Name
HYDROPHILIC COATED GUIDEWIRE
K Number
K926344
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Surgitek
Date Received
December 17, 1992
Decision Date
March 5, 1993
Product Code
KNY
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
KNY Accessories, Catheter, G-U

Similar 510(k) Clearances

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

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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
K930483 URETERAL CATHETER
K920451 ENDOTEK ULTRA SYSTEM
K922542 GRASPING FORCEPS
Search all 29 clearances from Surgitek →