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FDA 510(k)

MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR

K-Number: K874076 · 1988-01-04

ApplicantPhysio Technology, Inc.
Decision Date1988-01-04
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Physio Technology, Inc.. It received FDA 510(k) clearance on 1988-01-04 under 510(k) number K874076. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR?

MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1988-01-04. The listed applicant is Physio Technology, Inc.. The 510(k) number is K874076.

When did MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR receive FDA 510(k) clearance?

MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR received FDA 510(k) clearance on 1988-01-04, under 510(k) number K874076.

Who is the listed applicant for MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR?

The FDA 510(k) record lists Physio Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR?

The FDA product code for MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR is IPF.

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Other records listing Physio Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K883893OMNISOUND(TM) 3000K861039OMNIVAC (VACUUM ELECTRODE SYSTEM)K850850AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATORK850851G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'SK850849MYOMETER EMG BIOFEEDBACK DEVICEK843351OMNISTIM II COMBIN. THERAPY SYS

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Related Devices (Code: IPF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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