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FDA 510(k)

CLASSIC NMS

K-Number: K021905 · 2002-09-05

Decision Date2002-09-05
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLASSIC NMS is the device name listed in this FDA 510(k) record. The listed applicant is Care Rehab, Inc.. It received FDA 510(k) clearance on 2002-09-05 under 510(k) number K021905. 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 CLASSIC NMS?

CLASSIC NMS is a medical device that received FDA 510(k) clearance on 2002-09-05. The listed applicant is Care Rehab, Inc.. The 510(k) number is K021905.

When did CLASSIC NMS receive FDA 510(k) clearance?

CLASSIC NMS received FDA 510(k) clearance on 2002-09-05, under 510(k) number K021905.

Who is the listed applicant for CLASSIC NMS?

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

What is the FDA product code for CLASSIC NMS?

The FDA product code for CLASSIC NMS 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.

Other records listing Care Rehab, Inc. 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.

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.

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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