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FDA 510(k)

SHARP COLLECTION SYSTEM-SHARP-A-GATOR

K-Number: K844654 · 1984-12-12

Decision Date1984-12-12
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARP COLLECTION SYSTEM-SHARP-A-GATOR is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1984-12-12 under 510(k) number K844654. 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 SHARP COLLECTION SYSTEM-SHARP-A-GATOR?

SHARP COLLECTION SYSTEM-SHARP-A-GATOR is a medical device that received FDA 510(k) clearance on 1984-12-12. The listed applicant is Devon Industries, Inc.. The 510(k) number is K844654.

When did SHARP COLLECTION SYSTEM-SHARP-A-GATOR receive FDA 510(k) clearance?

SHARP COLLECTION SYSTEM-SHARP-A-GATOR received FDA 510(k) clearance on 1984-12-12, under 510(k) number K844654.

Who is the listed applicant for SHARP COLLECTION SYSTEM-SHARP-A-GATOR?

The FDA 510(k) record lists Devon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARP COLLECTION SYSTEM-SHARP-A-GATOR?

The FDA product code for SHARP COLLECTION SYSTEM-SHARP-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 Devon Industries, 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.

View all 47 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

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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