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FDA 510(k)

SHARPS DISPOSAL CONTAINERS

K-Number: K953797 · 1995-11-27

ApplicantBemis Mfg. Co.
Decision Date1995-11-27
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS DISPOSAL 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 1995-11-27 under 510(k) number K953797. 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 DISPOSAL CONTAINERS?

SHARPS DISPOSAL CONTAINERS is a medical device that received FDA 510(k) clearance on 1995-11-27. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K953797.

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

SHARPS DISPOSAL CONTAINERS received FDA 510(k) clearance on 1995-11-27, under 510(k) number K953797.

Who is the listed applicant for SHARPS DISPOSAL 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 DISPOSAL CONTAINERS?

The FDA product code for SHARPS DISPOSAL 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.

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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.

K020921NO-POKES NEEDLE SAFETY DEVICEK965248BEMIS TWO GALLON SHARPS CONTAINERK964858BEMIS TWO GALLON CHEMOTHERAPY CONTAINERK960525BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)K950340IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERSK941664SHARP DISPOSAL CONTAINERS WALL SAFE

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.

K260845Huahong Sharps Container (HHR-I, HHR-II)Tianjin Huahong Technology Co., Ltd.K253773Guanhong Sharps Container (GHW-1F1); Guanhong Sharps Container (GHW-1F4); Guanhong Sharps Container (GH-6FA); Guanhong Sharps Container (GHW-2FR); Guanhong Sharps Container (GHW-8FR); Guanhong Sharps Container (GH-3FS); Guanhong Sharps Container (GHW-15FS); Guanhong Sharps Container (GHW-27FS); Guanhong Sharps Container (GH-5FSW); Guanhong Sharps Container (GHW-3FT); Guanhong Sharps Container (GHW-4FT); Guanhong Sharps Container (GHW-5FT); Guanhong Sharps Container (GHW-8FT); GuanhongTaizhou Huangyan Guanhong Plastic Steel Products FactoryK253222Gongdong Sharps Container (SCR-01Q, SCR-01G, SCR-03G)Zhejiang Gongdong Medical Technology Co., Ltd.K251874PureWay Sharps Container 1-Gal, 2-Gal, 3-Gal (800011 800012, 800013)Pureway Compliance, Inc.K252637Community Containers (Flap and Daisy)Keter Canada, Inc.K231484PureWay 1.4 Quart Sharps CollectorPureway Compliance, Inc.

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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