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

FUJINON EVL-F (TENTATIVE) AND TROCAR

K Number: K902197 · Decision Mar 5, 1991
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
30
Review Days
293

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Basic Information

Device Name
FUJINON EVL-F (TENTATIVE) AND TROCAR
K Number
K902197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Fujinon, Inc.
Date Received
May 16, 1990
Decision Date
March 5, 1991
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

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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. →