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FDA 510(k)

PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY

K-Number: K893513 · 1989-12-11

ApplicantPioneer Sundries Products , Ltd.
Decision Date1989-12-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Sundries Products , Ltd.. It received FDA 510(k) clearance on 1989-12-11 under 510(k) number K893513. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY?

PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY is a medical device that received FDA 510(k) clearance on 1989-12-11. The listed applicant is Pioneer Sundries Products , Ltd.. The 510(k) number is K893513.

When did PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY received FDA 510(k) clearance on 1989-12-11, under 510(k) number K893513.

Who is the listed applicant for PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY?

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

What is the FDA product code for PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY?

The FDA product code for PATIENT EXAMINATION GLOVE/MANUF. KUN SHAN FACTORY is LYY.

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Other records listing Pioneer Sundries Products , Ltd. 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.

K910891PVC VINYL GLOVE

Related Devices (Code: LYY)

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.

K250069Powder Free Natural Rubber Latex Examination Gloves – Blue, Non-Sterile and Protein Claim Of 50 Micrograms per dm2 Or Less ProteinComfort Rubber Gloves Industries Sdn. Bhd.K240266Latex Examination Glove Powder Free (Ocean Blue and Natural White)Sri Trang Gloves (Thailand) Public Company LimitedK230573Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein)Kossan International Sdn BhdK223298Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L)Shandong Intco Medical Products Co, Ltd.K222612Powder-Free Latex examination glovesGuangdong Kingfa Sci. & Tech.Co., Ltd.K221667Non Sterile Powder Free Latex Examination GloveNew Era Medicare Sdn. Bhd.

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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