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FDA 510(k)

ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID

K-Number: K875317 · 1989-09-08

ApplicantElectro Therapeutic Devices, Inc.
Decision Date1989-09-08
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID is the device name listed in this FDA 510(k) record. The listed applicant is Electro Therapeutic Devices, Inc.. It received FDA 510(k) clearance on 1989-09-08 under 510(k) number K875317. 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 ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID?

ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID is a medical device that received FDA 510(k) clearance on 1989-09-08. The listed applicant is Electro Therapeutic Devices, Inc.. The 510(k) number is K875317.

When did ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID receive FDA 510(k) clearance?

ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID received FDA 510(k) clearance on 1989-09-08, under 510(k) number K875317.

Who is the listed applicant for ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID?

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

What is the FDA product code for ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID?

The FDA product code for ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID is IPF.

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Other records listing Electro Therapeutic Devices, 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.

K981272ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLESK863567'TENSAID'K863568'MYOSTIM EX'K853718TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 804K853719TRANSCUTANEOUS ELECT. NERVE STIMUL-MYOSTIM 410K843119ETI TENS BELT

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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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