Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CARDON PHYSICAL THERAPY TABLE R27114 AND R27642

K-Number: K950362 · 1995-02-10

Decision Date1995-02-10
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARDON PHYSICAL THERAPY TABLE R27114 AND R27642 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 1995-02-10 under 510(k) number K950362. 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 PHYSICAL THERAPY TABLE R27114 AND R27642?

CARDON PHYSICAL THERAPY TABLE R27114 AND R27642 is a medical device that received FDA 510(k) clearance on 1995-02-10. The listed applicant is Cardon Rehabilitation Products, Inc.. The 510(k) number is K950362.

When did CARDON PHYSICAL THERAPY TABLE R27114 AND R27642 receive FDA 510(k) clearance?

CARDON PHYSICAL THERAPY TABLE R27114 AND R27642 received FDA 510(k) clearance on 1995-02-10, under 510(k) number K950362.

Who is the listed applicant for CARDON PHYSICAL THERAPY TABLE R27114 AND R27642?

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 PHYSICAL THERAPY TABLE R27114 AND R27642?

The FDA product code for CARDON PHYSICAL THERAPY TABLE R27114 AND R27642 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑