FDA 510(k)

SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE

K-Number: K011765 · 2001-08-16

ApplicantSunmax Enterprise Shanghai Co. , Ltd.

Decision Date2001-08-16

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Sunmax Enterprise Shanghai Co. , Ltd.. It received FDA 510(k) clearance on 2001-08-16 under 510(k) number K011765. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE?

SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2001-08-16. The listed applicant is Sunmax Enterprise Shanghai Co. , Ltd.. The 510(k) number is K011765.

When did SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE receive FDA 510(k) clearance?

SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE received FDA 510(k) clearance on 2001-08-16, under 510(k) number K011765.

Who is the listed applicant for SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE?

The FDA 510(k) record lists Sunmax Enterprise Shanghai Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE?

The FDA product code for SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE is LZA.

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 Sunmax Enterprise Shanghai Co. , Ltd. as applicant

K090336SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS K011717SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVES K964964POWDER-FREE VINYL PATIENT EXAMINATION GLOVES K960746SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES

Related Devices (Code: LZA)

K261793Powder-free Nitrile Examination Gloves Tested for Use With Chemotherapy Drugs and Fentanyl Citrate (Blue and Black Color)Maxter Healthcare, Inc.K262542Biodegradable Nitrile Powder Free Examination Glove, Green; Biodegradable Nitrile Powder Free Examination Glove, Violet Blue Tested for Use With 32 Chemotherapy Drugs, Fentanyl & Gastric Acid Permeation Resistance ClaimTop Glove Sdn. Bhd.K260312Nitrile Powder Free Examination Glove, Blue Tested for Use with 32 Chemotherapy Drugs and Fentanyl Permeation Resistance Claim; Nitrile Powder Free Examination Glove, Violet Blue Tested for Use with 32 Chemotherapy Drugs, Xylazine, Fentanyl & Gastric AcidGmp Medicare Sdn. Bhd.K261749Cardinal Health Nitrile Blue Examination Gloves Tested for Use with Chemotherapy Drugs and Fentanyl CitrateCardinalhealth K260794NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WITH LICORICE ROOT EXTRACT AND UREA, TESTED FOR USE WITH CHEMOTHERAPY DRUGS, FENTANYL CITRATE, XYLAZINE HCl, AND GASTRIC ACID. OCEAN COLORKossan International Sdn Bhd K262014PUREZERO* MARIN* Nitrile Powder-Free Exam Gloves; PUREZERO* MARIN-XTRA* Nitrile Powder-Free Exam GlovesO&M Halyard, 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.