RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL)
K-Number: K891843 · 1989-06-06
Advertisement
Device Summary
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.
Advertisement