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FDA 510(k)

HOYER DIGITAL ELECTRONIC SCALE

K-Number: K862477 · 1986-09-03

Decision Date1986-09-03
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HOYER DIGITAL ELECTRONIC SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Ted Hoyer & Co., Inc.. It received FDA 510(k) clearance on 1986-09-03 under 510(k) number K862477. 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 HOYER DIGITAL ELECTRONIC SCALE?

HOYER DIGITAL ELECTRONIC SCALE is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Ted Hoyer & Co., Inc.. The 510(k) number is K862477.

When did HOYER DIGITAL ELECTRONIC SCALE receive FDA 510(k) clearance?

HOYER DIGITAL ELECTRONIC SCALE received FDA 510(k) clearance on 1986-09-03, under 510(k) number K862477.

Who is the listed applicant for HOYER DIGITAL ELECTRONIC SCALE?

The FDA 510(k) record lists Ted Hoyer & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOYER DIGITAL ELECTRONIC SCALE?

The FDA product code for HOYER DIGITAL ELECTRONIC 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 Ted Hoyer & Co., Inc. 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.

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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