FDA 510(k)

CARE STIM

K-Number: K022417 · 2003-04-10

Decision Date2003-04-10

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CARE 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 2003-04-10 under 510(k) number K022417. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARE STIM?

CARE STIM is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Care Rehab and Orthopaedic. The 510(k) number is K022417.

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

CARE STIM received FDA 510(k) clearance on 2003-04-10, under 510(k) number K022417.

Who is the listed applicant for CARE 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 CARE STIM?

The FDA product code for CARE STIM is GZJ.

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 ETS K020637SELECT STIM

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K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimed K252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLC K232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical Officer K233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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.