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FDA 510(k)

BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F

K-Number: K903723 · 1990-09-24

Decision Date1990-09-24
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F is the device name listed in this FDA 510(k) record. The listed applicant is Barrier Free Lifts, Inc.. It received FDA 510(k) clearance on 1990-09-24 under 510(k) number K903723. The device is classified under product code FNG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F?

BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F is a medical device that received FDA 510(k) clearance on 1990-09-24. The listed applicant is Barrier Free Lifts, Inc.. The 510(k) number is K903723.

When did BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F receive FDA 510(k) clearance?

BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F received FDA 510(k) clearance on 1990-09-24, under 510(k) number K903723.

Who is the listed applicant for BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F?

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

What is the FDA product code for BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F?

The FDA product code for BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F is FNG.

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: FNG)

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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