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FDA 510(k)

DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL

K-Number: K792016 · 1979-10-26

Decision Date1979-10-26
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL is the device name listed in this FDA 510(k) record. The listed applicant is Arbrook Mfg. Corp.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K792016. 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 DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL?

DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Arbrook Mfg. Corp.. The 510(k) number is K792016.

When did DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL receive FDA 510(k) clearance?

DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL received FDA 510(k) clearance on 1979-10-26, under 510(k) number K792016.

Who is the listed applicant for DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL?

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

What is the FDA product code for DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL?

The FDA product code for DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL 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 Arbrook Mfg. 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.

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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