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

LAPAROFLATOR 3000, STANDARD AND ELECTRONIC

K Number: K875137 · Decision Mar 2, 1988
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
12
Applicant Total
12
Review Days
78

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Basic Information

Device Name
LAPAROFLATOR 3000, STANDARD AND ELECTRONIC
K Number
K875137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
F.M. Wiest USA, Inc.
Date Received
December 15, 1987
Decision Date
March 2, 1988
Product Code
HES
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
HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by F.M. Wiest USA, Inc.

K Number Device Name
K921871 HYSTEROMAT(TM) 3700
K920574 CAMSYS 6300
K920575 MERKUR 4000
K915751 URETEROMAT 4400
K911844 HYSTEROFLATOR 1500
K912071 SPACE(TM) 7500
K910883 LAPAROFLATOR ELECTRONIC 3509
K871181 ARTHROCOMBI 5003
K871180 ARTHRO AUTOMAT 5002
K865066 ARTHROFLATOR
Search all 12 clearances from F.M. Wiest USA, Inc. →