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

FLEXIBLE FIBER OPTIC LAPAROSCOPES

K Number: K943598 · Decision Oct 18, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
15
Review Days
84

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Basic Information

Device Name
FLEXIBLE FIBER OPTIC LAPAROSCOPES
K Number
K943598
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Optimed Technologies, Inc.
Date Received
July 26, 1994
Decision Date
October 18, 1994
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 Optimed Technologies, Inc.

K Number Device Name
K972520 OPTIVIEW
K955275 BOOSTER TROPHY 5 MOTORIZED SCOOTER
K955276 BOOSTER LITE 4 MOTORIZED SCOOTER
K955274 BOOSTER LITE 3 MOTORIZED SCOOTER
K926597 LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
K921942 HYSTEROSCOPE (AND ACCESSORIES)
K922711 FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE
K921985 ARTHROSCOPE & ACCESSORIES
K922826 FLEXIBLE FIBER OPTIC ENDOSCOPE
K921883 ENDOSCOPE
Search all 15 clearances from Optimed Technologies, Inc. →