PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES)
K-Number: K891815 · 1989-08-15
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES)?
PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES) is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Mulpha Intl. Trading Corp. Bhd.. The 510(k) number is K891815.
When did PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES) received FDA 510(k) clearance on 1989-08-15, under 510(k) number K891815.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES)?
The FDA 510(k) record lists Mulpha Intl. Trading Corp. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES)?
The FDA product code for PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES) 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 Mulpha Intl. Trading Corp. Bhd. 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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