FDA 510(k)

PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE)

K-Number: K962650 · 1996-08-15

Decision Date1996-08-15

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Sti Medical Sdn Bhd. It received FDA 510(k) clearance on 1996-08-15 under 510(k) number K962650. 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 LATEX EXAMINATION GLOVES (POWDERED, NON STERILE)?

PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Sti Medical Sdn Bhd. The 510(k) number is K962650.

When did PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) receive FDA 510(k) clearance?

PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) received FDA 510(k) clearance on 1996-08-15, under 510(k) number K962650.

Who is the listed applicant for PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE)?

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

What is the FDA product code for PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE)?

The FDA product code for PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE) 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 Sti Medical Sdn Bhd as applicant

K970613PATIENT EXAMINATION GLOVES (POWDER FREE-NON STERILE)

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

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