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FDA 510(k)

U.S. MEDICAL PS-2000 PEDIATRIC SCALE

K-Number: K910582 · 1991-03-21

Decision Date1991-03-21
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

U.S. MEDICAL PS-2000 PEDIATRIC SCALE is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Medical Corp.. It received FDA 510(k) clearance on 1991-03-21 under 510(k) number K910582. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U.S. MEDICAL PS-2000 PEDIATRIC SCALE?

U.S. MEDICAL PS-2000 PEDIATRIC SCALE is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is U.S. Medical Corp.. The 510(k) number is K910582.

When did U.S. MEDICAL PS-2000 PEDIATRIC SCALE receive FDA 510(k) clearance?

U.S. MEDICAL PS-2000 PEDIATRIC SCALE received FDA 510(k) clearance on 1991-03-21, under 510(k) number K910582.

Who is the listed applicant for U.S. MEDICAL PS-2000 PEDIATRIC SCALE?

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

What is the FDA product code for U.S. MEDICAL PS-2000 PEDIATRIC SCALE?

The FDA product code for U.S. MEDICAL PS-2000 PEDIATRIC SCALE is FRW.

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 U.S. Medical Corp. 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 8 devices →

Related Devices (Code: FRW)

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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