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FDA 510(k)

AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR

K-Number: K850850 · 1985-07-01

ApplicantPhysio Technology, Inc.
Decision Date1985-07-01
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

AUTOMOVE/OMNISTIM IV-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 1985-07-01 under 510(k) number K850850. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR?

AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Physio Technology, Inc.. The 510(k) number is K850850.

When did AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR receive FDA 510(k) clearance?

AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR received FDA 510(k) clearance on 1985-07-01, under 510(k) number K850850.

Who is the listed applicant for AUTOMOVE/OMNISTIM IV-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 AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR?

The FDA product code for AUTOMOVE/OMNISTIM IV-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) 3000K874076MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATORK861039OMNIVAC (VACUUM ELECTRODE SYSTEM)K850851G5 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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