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FDA 510(k)

ADVANCED IN-BED WEIGH SYSTEM

K-Number: K943587 · 1994-09-22

Decision Date1994-09-22
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADVANCED IN-BED WEIGH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Future Systems, Inc.. It received FDA 510(k) clearance on 1994-09-22 under 510(k) number K943587. 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 ADVANCED IN-BED WEIGH SYSTEM?

ADVANCED IN-BED WEIGH SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-22. The listed applicant is Future Systems, Inc.. The 510(k) number is K943587.

When did ADVANCED IN-BED WEIGH SYSTEM receive FDA 510(k) clearance?

ADVANCED IN-BED WEIGH SYSTEM received FDA 510(k) clearance on 1994-09-22, under 510(k) number K943587.

Who is the listed applicant for ADVANCED IN-BED WEIGH SYSTEM?

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

What is the FDA product code for ADVANCED IN-BED WEIGH SYSTEM?

The FDA product code for ADVANCED IN-BED WEIGH SYSTEM 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.

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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