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

FUJINON VIDEO LAPORASCOPE

K Number: K933544 · Decision Apr 27, 1995
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
30
Review Days
644

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Basic Information

Device Name
FUJINON VIDEO LAPORASCOPE
K Number
K933544
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fujinon, Inc.
Date Received
July 22, 1993
Decision Date
April 27, 1995
Product Code
HIH
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
HIH Hysteroscope (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Fujinon, Inc.

K Number Device Name
K120446 FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2
K112391 FUJINON COLONOSCOPES
K102466 FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR
K111243 FUJINON ULTRASONIC PROCESSOR
K091773 FUJINON STERILE OVERTUBES
K090116 FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15
K063316 FUJINON MODEL EG-530N TRANS NASAL INSERTION
K063847 FUJINON ULTRASONIC ENDOSCOPE AND PROCESSOR, MODELS EG-530UR, EG-530UT AND SU-700
K050907 FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P
K042043 FUJINON INC. G5 GASTROSCOPES, MODELS EC-450WR5, EC-250WR5
Search all 30 clearances from Fujinon, Inc. →