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FDA 510(k)

RESTRAINING STRETCHER

K-Number: K924275 · 1993-07-27

ApplicantDms
Decision Date1993-07-27
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RESTRAINING STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Dms. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K924275. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESTRAINING STRETCHER?

RESTRAINING STRETCHER is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Dms. The 510(k) number is K924275.

When did RESTRAINING STRETCHER receive FDA 510(k) clearance?

RESTRAINING STRETCHER received FDA 510(k) clearance on 1993-07-27, under 510(k) number K924275.

Who is the listed applicant for RESTRAINING STRETCHER?

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

What is the FDA product code for RESTRAINING STRETCHER?

The FDA product code for RESTRAINING STRETCHER is FPP.

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.

Related Devices (Code: FPP)

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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