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FDA 510(k)

HEALTH PULSE FA-222 POWER MUSCLE STIMUL

K-Number: K843638 · 1984-11-23

ApplicantTherapeutic Equipment Corp.
Decision Date1984-11-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEALTH PULSE FA-222 POWER MUSCLE STIMUL is the device name listed in this FDA 510(k) record. The listed applicant is Therapeutic Equipment Corp.. It received FDA 510(k) clearance on 1984-11-23 under 510(k) number K843638. 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 HEALTH PULSE FA-222 POWER MUSCLE STIMUL?

HEALTH PULSE FA-222 POWER MUSCLE STIMUL is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is Therapeutic Equipment Corp.. The 510(k) number is K843638.

When did HEALTH PULSE FA-222 POWER MUSCLE STIMUL receive FDA 510(k) clearance?

HEALTH PULSE FA-222 POWER MUSCLE STIMUL received FDA 510(k) clearance on 1984-11-23, under 510(k) number K843638.

Who is the listed applicant for HEALTH PULSE FA-222 POWER MUSCLE STIMUL?

The FDA 510(k) record lists Therapeutic Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEALTH PULSE FA-222 POWER MUSCLE STIMUL?

The FDA product code for HEALTH PULSE FA-222 POWER MUSCLE STIMUL is IPF.

Related Clinical Trials

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.

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Other records listing Therapeutic Equipment Corp. 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.

K862846TEC VARI-TRAC II TRACTION UNITK852065PRESTON LOWER LIMB CPM UNITK843637HEALTH PULSE FA-222 TRANSCUTANEOUS ELEC. NERVE STI

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

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

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