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

ELECTRODES (BLADE, BALL, NEEDLE, AND LOOP)

K Number: K942986 · Decision Mar 21, 1995
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
52
Applicant Total
46
Review Days
293

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Basic Information

Device Name
ELECTRODES (BLADE, BALL, NEEDLE, AND LOOP)
K Number
K942986
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4120
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Aaron Medical Industries
Date Received
June 1, 1994
Decision Date
March 21, 1995
Product Code
HGI
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HGI Electrocautery, Gynecologic (And Accessories)

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Other Clearances by Aaron Medical Industries

K Number Device Name
K062337 MODULAR LAPAROSCOPY ACCESSORIES, HANDLE; SISSORS (STRAIGHT AND CURVED); GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC; DISSECTOR
K061307 BOVIE INAFLASH SUTURE REMOVER HANDLE,CHARGER,HANDLE AND CHARGER,KIT,BATTERY PACK
K060117 BOVIE BUTTON REMOTE HAND SWITCH
K022856 BOVIE IDS-300 HIGH FREQUENCY ELECTROSURGICAL GENERATOR
K021817 AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V
K020579 AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03
K014201 AARON REUSABLE ELECTROSURGICAL ELECTRODE
K001955 AARON 1250 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, MODEL A1250
K001382 AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR
K000961 AARON 900 HIGH FREQUENCY DESSICCATOR/HANDPIECE
Search all 46 clearances from Aaron Medical Industries →