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)

MAYTEX NON-STERILE LATEX EXAM GLOVES

K-Number: K892082 · 1989-05-31

ApplicantMaytex Corp.
Decision Date1989-05-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAYTEX NON-STERILE LATEX EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Maytex Corp.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K892082. 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 MAYTEX NON-STERILE LATEX EXAM GLOVES?

MAYTEX NON-STERILE LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is Maytex Corp.. The 510(k) number is K892082.

When did MAYTEX NON-STERILE LATEX EXAM GLOVES receive FDA 510(k) clearance?

MAYTEX NON-STERILE LATEX EXAM GLOVES received FDA 510(k) clearance on 1989-05-31, under 510(k) number K892082.

Who is the listed applicant for MAYTEX NON-STERILE LATEX EXAM GLOVES?

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

What is the FDA product code for MAYTEX NON-STERILE LATEX EXAM GLOVES?

The FDA product code for MAYTEX NON-STERILE LATEX 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 Maytex Corp. 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.

↑