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

LAPAROSCOPY CONSOLE MODEL VIII

K Number: K772242 · Decision Dec 20, 1977
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
18
Review Days
12

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Basic Information

Device Name
LAPAROSCOPY CONSOLE MODEL VIII
K Number
K772242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Kli
Date Received
December 8, 1977
Decision Date
December 20, 1977
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HET), 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
K780955 SCISSORS, HOOK, ELECTROSURGICAL
K780954 SCISSORS, HOOK, ELECTROSURGICAL
K772297 INSUFFLATOR, MODEL G100 & 200
K772220 PROBE, COAGULATION ACCESSORY
K772185 LAPAROSCOPE W/REMOVABLE OPTICS
Search all 18 clearances from Kli →