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

VERIMED MYOEXORCISER III (MYO III)

K Number: K892649 · Decision Dec 13, 1989
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
171
Applicant Total
12
Review Days
245

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Basic Information

Device Name
VERIMED MYOEXORCISER III (MYO III)
K Number
K892649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5050
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Verimed Holdings, Inc.
Date Received
April 12, 1989
Decision Date
December 13, 1989
Product Code
HCC
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HCC Device, Biofeedback

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HCC), 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
K874212 VERIMED MYO/PREMS
K854193 ELECTRO-MYOGRAPHIC PERINEOMETER
K852963 MYO-ACTUATOR
Search all 12 clearances from Verimed Holdings, Inc. →