Therapeutic Stimulator 300(TS-300) & 300P(TS-300P)

FDA 510(k) K932764 · Myo/Kinetic Systems, Inc.

Substantially Equivalent

510(k) numberK932764

Submission

Device name
Therapeutic Stimulator 300(TS-300) & 300P(TS-300P)
Applicant
Myo/Kinetic Systems, Inc.
Menomonee Falls, WI, US
Received
June 8, 1993
Decision date
October 1, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IPF – Stimulator, Muscle, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5850
Specialty
Physical Medicine

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More from Sunmed, LLC

510(k)DeviceDecision
K945937TE-800 Pelvic Floor ExerciserHIR · Traditional 07/14/1995SE
K945292TS-700P Control XP Electrical StimulatorKPI · Traditional 04/12/1995SE
K944972Uro-Gram Cystomrtrogram with UroflowmetryEXY · Traditional 03/08/1995SE
K936041Urogram CystometrogramFEN · Traditional 04/18/1994SE
K932611Neuromuscular StimulatorGZJ · Traditional 01/31/1994SE
K932399Therapeutic Stim 200 (TS-200)/200P (TS-200P)IPF · Traditional 08/11/1993SE
K914904Therapeutic Stimulator 2100 (TS-2100)IPF · Traditional 04/28/1992SE

Questions and answers

When was Therapeutic Stimulator 300(TS-300) & 300P(TS-300P) cleared by the FDA?

Therapeutic Stimulator 300(TS-300) & 300P(TS-300P) (K932764) received a 510(k) decision of Substantially Equivalent on October 1, 1993, 115 days after the submission was received.

What is the product code of K932764?

The FDA product code is IPF – Stimulator, Muscle, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5850.