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FDA 510(k)

CARDON PHSICAL THERAPY TABLE MODEL R27630

K-Number: K951953 · 1995-05-31

Decision Date1995-05-31
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARDON PHSICAL THERAPY TABLE MODEL R27630 is the device name listed in this FDA 510(k) record. The listed applicant is Cardon Rehabilitation Products, Inc.. It received FDA 510(k) clearance on 1995-05-31 under 510(k) number K951953. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDON PHSICAL THERAPY TABLE MODEL R27630?

CARDON PHSICAL THERAPY TABLE MODEL R27630 is a medical device that received FDA 510(k) clearance on 1995-05-31. The listed applicant is Cardon Rehabilitation Products, Inc.. The 510(k) number is K951953.

When did CARDON PHSICAL THERAPY TABLE MODEL R27630 receive FDA 510(k) clearance?

CARDON PHSICAL THERAPY TABLE MODEL R27630 received FDA 510(k) clearance on 1995-05-31, under 510(k) number K951953.

Who is the listed applicant for CARDON PHSICAL THERAPY TABLE MODEL R27630?

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

What is the FDA product code for CARDON PHSICAL THERAPY TABLE MODEL R27630?

The FDA product code for CARDON PHSICAL THERAPY TABLE MODEL R27630 is INQ.

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 Cardon Rehabilitation Products, 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.

View all 16 devices →

Related Devices (Code: INQ)

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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