FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

MYOTRAC2D/CS

K Number: K925681 · Decision Sep 29, 1995
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
22
Review Days
1081

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Basic Information

Device Name
MYOTRAC2D/CS
K Number
K925681
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1425
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Thought Technology , Ltd.
Date Received
October 13, 1992
Decision Date
September 29, 1995
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 Thought Technology , Ltd.

K Number Device Name
K213197 MyOnyx System
K201014 MyOnyx System
K053434 MYOTRAC INFINITI ELECTRICAL STIMULATOR
K053266 MYOTRAC INFINITI
K932149 THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE
K935213 INCONTROL
K915858 MYOTRAC2
K915859 MYOTRAC/S, MYODAC/S
K913898 MYOTRAC+/S, MYODAC+/S
K903497 FLEXCOMP DSP & PROCOMP
Search all 22 clearances from Thought Technology , Ltd. →