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

BTM-200 (PROPOSED) POWERED MUSCLE STIMULATOR

K Number: K915321 · Decision Jul 17, 1992
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
5
Review Days
238

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Basic Information

Device Name
BTM-200 (PROPOSED) POWERED MUSCLE STIMULATOR
K Number
K915321
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bt Medical Co., Inc.
Date Received
November 22, 1991
Decision Date
July 17, 1992
Product Code
IPF
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IPF Stimulator, Muscle, Powered

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Other Clearances by Bt Medical Co., Inc.

K Number Device Name
K931268 URETERAL COMPRESSION DEVICE
K930885 PNEUMATIC COMPRESSION DEVICE
K931269 LEAD APRON
K914999 BTM-100 POWERED MUSCLE STIMULATOR (PROPOSED)