FDA 510(k)

PVC PATIENT EXAMINATION GLOVE

K-Number: K902278 · 1990-08-29

Decision Date1990-08-29

Product CodeFMC

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PVC PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Fujian Province Jiu Zhou Group. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K902278. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVC PATIENT EXAMINATION GLOVE?

PVC PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Fujian Province Jiu Zhou Group. The 510(k) number is K902278.

When did PVC PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

PVC PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1990-08-29, under 510(k) number K902278.

Who is the listed applicant for PVC PATIENT EXAMINATION GLOVE?

The FDA 510(k) record lists Fujian Province Jiu Zhou Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PVC PATIENT EXAMINATION GLOVE?

The FDA product code for PVC PATIENT EXAMINATION GLOVE is FMC.

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

Related Devices (Code: FMC)

K042618LAGLOVE BRAND DOUBLE POLYMER COATED NITRILE EXAMINATION GLOVES (POWDER FREE - BLUE COLOR)La Glove (M) Sdn. Bhd.K014134POWDER-FREE LATEX EXAM GLOVES WITH PROTEIN LABELING (<50UG/G)Supergrade Healthcare Products Sdn. Bhd.K992337BLOSSOM POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM 50 MCGM OR LESS OF TOTAL WATER EXTRACTAMexpo Intl., Inc.K932404NITRILE RUBBER POWDER-FREE EXAMINATION GLOVESafeskin Corp.K932405NITRILE RUBBER EXAMINATION GLOVES (POWERED)Safeskin Corp.K923175SURGICAL INSTRUMENT KIT, DISPOSABLEUlti-Med Intl., 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.