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FDA 510(k)

POINT OF USE II SHARPS-A-GATOR

K-Number: K964387 · 1997-03-27

Decision Date1997-03-27
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POINT OF USE II SHARPS-A-GATOR is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1997-03-27 under 510(k) number K964387. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POINT OF USE II SHARPS-A-GATOR?

POINT OF USE II SHARPS-A-GATOR is a medical device that received FDA 510(k) clearance on 1997-03-27. The listed applicant is Graphic Controls Corp.. The 510(k) number is K964387.

When did POINT OF USE II SHARPS-A-GATOR receive FDA 510(k) clearance?

POINT OF USE II SHARPS-A-GATOR received FDA 510(k) clearance on 1997-03-27, under 510(k) number K964387.

Who is the listed applicant for POINT OF USE II SHARPS-A-GATOR?

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

What is the FDA product code for POINT OF USE II SHARPS-A-GATOR?

The FDA product code for POINT OF USE II SHARPS-A-GATOR is MMK.

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 Graphic Controls 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 55 devices →

Related Devices (Code: MMK)

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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