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

SCISSORS, HOOK, ELECTROSURGICAL

K Number: K780955 · Decision Jun 22, 1978
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
43
Applicant Total
18
Review Days
13

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Basic Information

Device Name
SCISSORS, HOOK, ELECTROSURGICAL
K Number
K780955
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Kli
Date Received
June 9, 1978
Decision Date
June 22, 1978
Product Code
KNF
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
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Kli

K Number Device Name
K800822 CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE
K800913 GYNECOLOGICAL CYSTO/URETHROSCOPE
K781913 INSUFFALATOR LAPARAOSCOPIC
K781109 FORCEPS, ELECTROSURGICAL
K781089 ONE INCISION BI-POLAR ELECTRO. FORCEPS
K780954 SCISSORS, HOOK, ELECTROSURGICAL
K772297 INSUFFLATOR, MODEL G100 & 200
K772242 LAPAROSCOPY CONSOLE MODEL VIII
K772220 PROBE, COAGULATION ACCESSORY
K772185 LAPAROSCOPE W/REMOVABLE OPTICS
Search all 18 clearances from Kli →