FDA 510(k)

MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE

K-Number: K982877 · 1998-11-30

Decision Date1998-11-30

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Matang Mfg. Sdn. Bhd.. It received FDA 510(k) clearance on 1998-11-30 under 510(k) number K982877. 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 MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE?

MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1998-11-30. The listed applicant is Matang Mfg. Sdn. Bhd.. The 510(k) number is K982877.

When did MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1998-11-30, under 510(k) number K982877.

Who is the listed applicant for MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE?

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

What is the FDA product code for MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE?

The FDA product code for MATANG POWDER-FREE LOW PROTEIN LATEX PATIENT EXAMINATION GLOVE is LYY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Matang Mfg. Sdn. Bhd. as applicant

K122131POWDER FREE NITRILE EXAMINATION GLOVE-BLUE (CHEMOTHERAPY)K121368NITRILE EXAMINATION GLOVE, POWDER FREE (BLUE, BLACK OR WHITE)K072614MATANG BLACK, POWDER FREE AND POLYMER COATED LATEX EXAMINATION GLOVE K032549MATANG POWDER-FREE POLYCHLOROPRENE PATIENT EXAMINATION GLOVES K012558POWDER FREE LATEX PATIENT EXAMINATION GLOVES WITH ALOE VERA AND PROTEIN CONTENT LABELING CLAIM OF 50 MICROGRAMS OR LESS K000985MATANG POWDERED LATEX PATIENT EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS

View all 8 devices →

Related Devices (Code: LYY)

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 Limited K230573Powder 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 Bhd K223298Sterile 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.