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FDA 510(k)

HEEL/ELBOW FLOTATION CUSHION

K-Number: K760870 · 1976-11-01

ApplicantMedpro, Inc.
Decision Date1976-11-01
Product CodeFMP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEEL/ELBOW FLOTATION CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Medpro, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760870. The device is classified under product code FMP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEEL/ELBOW FLOTATION CUSHION?

HEEL/ELBOW FLOTATION CUSHION is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Medpro, Inc.. The 510(k) number is K760870.

When did HEEL/ELBOW FLOTATION CUSHION receive FDA 510(k) clearance?

HEEL/ELBOW FLOTATION CUSHION received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760870.

Who is the listed applicant for HEEL/ELBOW FLOTATION CUSHION?

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

What is the FDA product code for HEEL/ELBOW FLOTATION CUSHION?

The FDA product code for HEEL/ELBOW FLOTATION CUSHION is FMP.

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 Medpro, 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: FMP)

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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