PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.)
K-Number: K894178 · 1989-09-21
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.)?
PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.) is a medical device that received FDA 510(k) clearance on 1989-09-21. The listed applicant is Lanka Products, Inc.. The 510(k) number is K894178.
When did PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.) received FDA 510(k) clearance on 1989-09-21, under 510(k) number K894178.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.)?
The FDA 510(k) record lists Lanka Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.)?
The FDA product code for PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.) 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 Lanka Products, Inc. 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.
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