PATIENT EXAM GLOVES (MFG. KOON SENG)
K-Number: K893071 · 1990-05-21
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. KOON SENG)?
PATIENT EXAM GLOVES (MFG. KOON SENG) is a medical device that received FDA 510(k) clearance on 1990-05-21. The listed applicant is Innovative Medical Suppliers. The 510(k) number is K893071.
When did PATIENT EXAM GLOVES (MFG. KOON SENG) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. KOON SENG) received FDA 510(k) clearance on 1990-05-21, under 510(k) number K893071.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. KOON SENG)?
The FDA 510(k) record lists Innovative Medical Suppliers as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. KOON SENG)?
The FDA product code for PATIENT EXAM GLOVES (MFG. KOON SENG) 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 Innovative Medical Suppliers 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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