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

STARION CAUTERY HOOK

K Number: K000296 · Decision Mar 7, 2000
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
13
Review Days
36

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Basic Information

Device Name
STARION CAUTERY HOOK
K Number
K000296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Starion Instruments
Date Received
January 31, 2000
Decision Date
March 7, 2000
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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

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Other Clearances by Starion Instruments

K Number Device Name
K070871 STARION UNIVERSAL POWER SUPPLY
K062257 STARION INSTRUMENTS THERMAL LITIGATING SHEARS
K050308 THERMAL CAUTERY PROBE
K043155 STARION UNIVERSAL POWER SUPPLY (UPS)
K002547 STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR
K001273 STARION INSTRUMENTS POWER POINT CAUTERY CLAMP
K000893 AC POWERED THERMAL CAUTERY UNIT
K001262 THERMAL CAUTERY FORCEPS
K000250 CAUTERY FORCEPS WITH FOOTSWITCH
K994019 CAUTERY GRASPER/DISSECTOR
Search all 13 clearances from Starion Instruments →