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FDA 510(k)

SELECT STIM

K-Number: K020637 · 2002-05-28

ApplicantCare Rehab and Orthopaedic
Decision Date2002-05-28
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SELECT STIM is the device name listed in this FDA 510(k) record. The listed applicant is Care Rehab and Orthopaedic. It received FDA 510(k) clearance on 2002-05-28 under 510(k) number K020637. 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 SELECT STIM?

SELECT STIM is a medical device that received FDA 510(k) clearance on 2002-05-28. The listed applicant is Care Rehab and Orthopaedic. The 510(k) number is K020637.

When did SELECT STIM receive FDA 510(k) clearance?

SELECT STIM received FDA 510(k) clearance on 2002-05-28, under 510(k) number K020637.

Who is the listed applicant for SELECT STIM?

The FDA 510(k) record lists Care Rehab and Orthopaedic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELECT STIM?

The FDA product code for SELECT STIM is IPF.

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Other records listing Care Rehab and Orthopaedic 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.

K023036CARE ETSK022417CARE STIM

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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