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)

RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL)

K-Number: K891843 · 1989-06-06

Decision Date1989-06-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) is the device name listed in this FDA 510(k) record. The listed applicant is Worldwide Medical. It received FDA 510(k) clearance on 1989-06-06 under 510(k) number K891843. 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 RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL)?

RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) is a medical device that received FDA 510(k) clearance on 1989-06-06. The listed applicant is Worldwide Medical. The 510(k) number is K891843.

When did RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) receive FDA 510(k) clearance?

RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) received FDA 510(k) clearance on 1989-06-06, under 510(k) number K891843.

Who is the listed applicant for RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL)?

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

What is the FDA product code for RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL)?

The FDA product code for RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) 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 Worldwide Medical 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.

↑