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FDA 510(k)

SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER

K-Number: K942902 · 1994-12-15

ApplicantWinfield Co., Inc.
Decision Date1994-12-15
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Winfield Co., Inc.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K942902. 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-TAINER SMALL OPENING W/NEEDLE REMOVER?

SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Winfield Co., Inc.. The 510(k) number is K942902.

When did SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER receive FDA 510(k) clearance?

SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER received FDA 510(k) clearance on 1994-12-15, under 510(k) number K942902.

Who is the listed applicant for SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER?

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

What is the FDA product code for SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER?

The FDA product code for SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER 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 Winfield Co., 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.

K942901SHARPS-TAINER LARGE OPENINGK942903SHARPS-TAINER SMALL OPENINGK891855WINFIELD LATEX EXAMINATION GLOVESK802803CONVALESCENT RECLINER

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

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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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