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FDA 510(k)

DIGITAL BEDSIDE SCALE #5000

K-Number: K830171 · 1983-02-18

Decision Date1983-02-18
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL BEDSIDE SCALE #5000 is the device name listed in this FDA 510(k) record. The listed applicant is Acme Medical Scale Co.. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K830171. 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 DIGITAL BEDSIDE SCALE #5000?

DIGITAL BEDSIDE SCALE #5000 is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Acme Medical Scale Co.. The 510(k) number is K830171.

When did DIGITAL BEDSIDE SCALE #5000 receive FDA 510(k) clearance?

DIGITAL BEDSIDE SCALE #5000 received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830171.

Who is the listed applicant for DIGITAL BEDSIDE SCALE #5000?

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

What is the FDA product code for DIGITAL BEDSIDE SCALE #5000?

The FDA product code for DIGITAL BEDSIDE SCALE #5000 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 Acme Medical Scale Co. 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 10 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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