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FDA 510(k)

ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS

K-Number: K943659 · 1995-03-22

ApplicantSage Products, Inc.
Decision Date1995-03-22
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1995-03-22 under 510(k) number K943659. 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 ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS?

ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS is a medical device that received FDA 510(k) clearance on 1995-03-22. The listed applicant is Sage Products, Inc.. The 510(k) number is K943659.

When did ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS receive FDA 510(k) clearance?

ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS received FDA 510(k) clearance on 1995-03-22, under 510(k) number K943659.

Who is the listed applicant for ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS?

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

What is the FDA product code for ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS?

The FDA product code for ANCILLARY AND LARGE VOLUME SHARPS DISPOSAL CONTAINERS is MMK.

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Other records listing Sage Products, 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.

K972705RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTICK980490SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPSK9739112 GALLON ALTERNATE CARE SHARPS CONTAINERK972279SHARPS SHUTTLEK970135NITRILE GLOVESK972302POCKET COUNT OR SAFETCOUNT

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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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