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FDA 510(k)

SHARPS DISPOSABLE CONTAINERS

K-Number: K931664 · 1994-05-23

Decision Date1994-05-23
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS DISPOSABLE CONTAINERS is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Mfg. Co.. It received FDA 510(k) clearance on 1994-05-23 under 510(k) number K931664. 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 SHARPS DISPOSABLE CONTAINERS?

SHARPS DISPOSABLE CONTAINERS is a medical device that received FDA 510(k) clearance on 1994-05-23. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K931664.

When did SHARPS DISPOSABLE CONTAINERS receive FDA 510(k) clearance?

SHARPS DISPOSABLE CONTAINERS received FDA 510(k) clearance on 1994-05-23, under 510(k) number K931664.

Who is the listed applicant for SHARPS DISPOSABLE CONTAINERS?

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

What is the FDA product code for SHARPS DISPOSABLE CONTAINERS?

The FDA product code for SHARPS DISPOSABLE CONTAINERS 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 Bemis Mfg. Co. 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 12 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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