Cleared Traditional

K895760 - ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE

K895760 is an FDA 510(k) clearance for ELECTRICAL MUSCLE STIMULATOR--PGS 2000 ..., manufactured by Universal Technology Systems, Inc.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 98-day FDA review.

K895760 · Universal Technology Systems, Inc. · Physical Medicine device
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Jan 1990
Decision
98d
Days
Class 2
Risk

K895760 is an FDA 510(k) clearance for the ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Universal Technology Systems, Inc. (Jacksonville, US). The FDA issued a Cleared decision on January 2, 1990 after a review of 98 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Universal Technology Systems, Inc. devices

FDA 510(k) Submission Details - K895760

510(k) Number K895760 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 26, 1989
Decision Date January 02, 1990
Days to Decision 98 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 115d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.

Regulatory Peers - IPF Stimulator, Muscle, Powered

All 197
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K895760.
EMS 8100
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K893878 · Mettler Electronics Corp. · Dec 1989
SYS*STIM 207A
K893879 · Mettler Electronics Corp. · Dec 1989
IF2000 ELECTRICAL MUSCLE STIMULATOR UNIT
K893994 · Rich-Mar Corp. · Dec 1989