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 EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER

K-Number: K892675 · 1989-05-31

Decision Date1989-05-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER is the device name listed in this FDA 510(k) record. The listed applicant is T.C. Electronics Co.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K892675. 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 EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER?

PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is T.C. Electronics Co.. The 510(k) number is K892675.

When did PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER received FDA 510(k) clearance on 1989-05-31, under 510(k) number K892675.

Who is the listed applicant for PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER?

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

What is the FDA product code for PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER?

The FDA product code for PATIENT EXAM GLOVES (LATEX) MFG. ADVANCE RUBBER 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 T.C. Electronics 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.

↑