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)

SUNTEX STERILE EXAM GLOVES

K-Number: K910631 · 1991-03-07

Decision Date1991-03-07
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUNTEX STERILE EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is P.T. Latexindo Prautama. It received FDA 510(k) clearance on 1991-03-07 under 510(k) number K910631. 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 SUNTEX STERILE EXAM GLOVES?

SUNTEX STERILE EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1991-03-07. The listed applicant is P.T. Latexindo Prautama. The 510(k) number is K910631.

When did SUNTEX STERILE EXAM GLOVES receive FDA 510(k) clearance?

SUNTEX STERILE EXAM GLOVES received FDA 510(k) clearance on 1991-03-07, under 510(k) number K910631.

Who is the listed applicant for SUNTEX STERILE EXAM GLOVES?

The FDA 510(k) record lists P.T. Latexindo Prautama as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNTEX STERILE EXAM GLOVES?

The FDA product code for SUNTEX STERILE EXAM 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 P.T. Latexindo Prautama 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.

↑