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)

PATIENT EXAMINATION GLOVES (NATURAL LATEX)

K-Number: K891967 · 1989-07-14

Decision Date1989-07-14
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES (NATURAL LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is Butex Products (M'Sia) Sdn.Bhd. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K891967. 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 EXAMINATION GLOVES (NATURAL LATEX)?

PATIENT EXAMINATION GLOVES (NATURAL LATEX) is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Butex Products (M'Sia) Sdn.Bhd. The 510(k) number is K891967.

When did PATIENT EXAMINATION GLOVES (NATURAL LATEX) receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVES (NATURAL LATEX) received FDA 510(k) clearance on 1989-07-14, under 510(k) number K891967.

Who is the listed applicant for PATIENT EXAMINATION GLOVES (NATURAL LATEX)?

The FDA 510(k) record lists Butex Products (M'Sia) Sdn.Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMINATION GLOVES (NATURAL LATEX)?

The FDA product code for PATIENT EXAMINATION GLOVES (NATURAL LATEX) 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.

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.

↑