FDA 510(k)

CARE ETS

K-Number: K023036 · 2003-06-19

Decision Date2003-06-19

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

CARE ETS 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 2003-06-19 under 510(k) number K023036. 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 CARE ETS?

CARE ETS is a medical device that received FDA 510(k) clearance on 2003-06-19. The listed applicant is Care Rehab and Orthopaedic. The 510(k) number is K023036.

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

CARE ETS received FDA 510(k) clearance on 2003-06-19, under 510(k) number K023036.

Who is the listed applicant for CARE ETS?

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 ETS?

The FDA product code for CARE ETS is IPF.

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.

K022417CARE STIM K020637SELECT STIM

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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.