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FDA 510(k)

PMP MUSCLE STIMULATOR

K-Number: K924699 · 1993-04-30

ApplicantPreferred Medical Products
Decision Date1993-04-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PMP MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Medical Products. It received FDA 510(k) clearance on 1993-04-30 under 510(k) number K924699. 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 PMP MUSCLE STIMULATOR?

PMP MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1993-04-30. The listed applicant is Preferred Medical Products. The 510(k) number is K924699.

When did PMP MUSCLE STIMULATOR receive FDA 510(k) clearance?

PMP MUSCLE STIMULATOR received FDA 510(k) clearance on 1993-04-30, under 510(k) number K924699.

Who is the listed applicant for PMP MUSCLE STIMULATOR?

The FDA 510(k) record lists Preferred Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMP MUSCLE STIMULATOR?

The FDA product code for PMP MUSCLE STIMULATOR 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 Preferred Medical Products 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.

K941153EPI-SPINAL ANESTHESIA TRAYK920808OB/GYN DRAPEK904440LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITSK885278EPIDURAL ANESTHESIA TRAYK885277SPINAL ANESTHESIA TRAY

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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