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

ELECTRO-MYOGRAPHIC PERINEOMETER

K Number: K854193 · Decision Jun 9, 1986
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
12
Review Days
237

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Basic Information

Device Name
ELECTRO-MYOGRAPHIC PERINEOMETER
K Number
K854193
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1425
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Verimed Holdings, Inc.
Date Received
October 15, 1985
Decision Date
June 9, 1986
Product Code
HIR
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIR Perineometer

Similar 510(k) Clearances

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

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Other Clearances by Verimed Holdings, Inc.

K Number Device Name
K981277 PERIFORM
K954127 BIOFEEDBACK DEVICE
K951969 MYOEXORCISER II FUAL
K930670 PHYACTION 787
K922550 ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)
K913912 VERIMED PERINEOMETER
K893220 VERIMED MYOEXORCISER VERISTIM
K892649 VERIMED MYOEXORCISER III (MYO III)
K874212 VERIMED MYO/PREMS
K852963 MYO-ACTUATOR
Search all 12 clearances from Verimed Holdings, Inc. →