DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL
K-Number: K792016 · 1979-10-26
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement