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

UTS ELECTRICAL MUSCLE STIMULATION DEVICE-PGS 1500

K Number: K905107 · Decision Aug 19, 1991
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
3
Review Days
279

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Basic Information

Device Name
UTS ELECTRICAL MUSCLE STIMULATION DEVICE-PGS 1500
K Number
K905107
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Universal Technology Systems, Inc.
Date Received
November 13, 1990
Decision Date
August 19, 1991
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 Universal Technology Systems, Inc.

K Number Device Name
K980346 ELECTRICAL MUSCLE STIMULATOR DEVICE ( PGS-4000)
K895760 ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE