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FDA 510(k)

UTILITY SCISSORS DISPOSABLE ITEMS

K-Number: K843075 · 1984-09-05

Decision Date1984-09-05
Product CodeJOK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UTILITY SCISSORS DISPOSABLE ITEMS is the device name listed in this FDA 510(k) record. The listed applicant is Greene International Corp.. It received FDA 510(k) clearance on 1984-09-05 under 510(k) number K843075. 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 UTILITY SCISSORS DISPOSABLE ITEMS?

UTILITY SCISSORS DISPOSABLE ITEMS is a medical device that received FDA 510(k) clearance on 1984-09-05. The listed applicant is Greene International Corp.. The 510(k) number is K843075.

When did UTILITY SCISSORS DISPOSABLE ITEMS receive FDA 510(k) clearance?

UTILITY SCISSORS DISPOSABLE ITEMS received FDA 510(k) clearance on 1984-09-05, under 510(k) number K843075.

Who is the listed applicant for UTILITY SCISSORS DISPOSABLE ITEMS?

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

What is the FDA product code for UTILITY SCISSORS DISPOSABLE ITEMS?

The FDA product code for UTILITY SCISSORS DISPOSABLE ITEMS 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 Greene International 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 8 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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