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FDA 510(k)

SHEAR, PLASTIC HANDLE UTILITY S-475-7

K-Number: K770481 · 1977-04-29

Decision Date1977-04-29
Product CodeJOK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHEAR, PLASTIC HANDLE UTILITY S-475-7 is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1977-04-29 under 510(k) number K770481. The device is classified under product code JOK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEAR, PLASTIC HANDLE UTILITY S-475-7?

SHEAR, PLASTIC HANDLE UTILITY S-475-7 is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Acme United Corp.. The 510(k) number is K770481.

When did SHEAR, PLASTIC HANDLE UTILITY S-475-7 receive FDA 510(k) clearance?

SHEAR, PLASTIC HANDLE UTILITY S-475-7 received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770481.

Who is the listed applicant for SHEAR, PLASTIC HANDLE UTILITY S-475-7?

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

What is the FDA product code for SHEAR, PLASTIC HANDLE UTILITY S-475-7?

The FDA product code for SHEAR, PLASTIC HANDLE UTILITY S-475-7 is JOK.

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 United 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 27 devices →

Related Devices (Code: JOK)

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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