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FDA 510(k)

SCALE, DIGITAL CHAIR

K-Number: K790130 · 1979-02-01

Decision Date1979-02-01
Product CodeFRI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SCALE, DIGITAL CHAIR 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 1979-02-01 under 510(k) number K790130. The device is classified under product code FRI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCALE, DIGITAL CHAIR?

SCALE, DIGITAL CHAIR is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Acme Medical Scale Co.. The 510(k) number is K790130.

When did SCALE, DIGITAL CHAIR receive FDA 510(k) clearance?

SCALE, DIGITAL CHAIR received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790130.

Who is the listed applicant for SCALE, DIGITAL CHAIR?

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 SCALE, DIGITAL CHAIR?

The FDA product code for SCALE, DIGITAL CHAIR is FRI.

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: FRI)

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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