Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

K-Number: K896957 · 1990-01-26

Decision Date1990-01-26
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Honyee Enterprise Co.. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K896957. 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 POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Honyee Enterprise Co.. The 510(k) number is K896957.

When did POWDER-FREE VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1990-01-26, under 510(k) number K896957.

Who is the listed applicant for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?

The FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES 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.

Other records listing Honyee Enterprise Co. 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.

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.

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.

↑