PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES)
K-Number: K892030 · 1989-05-01
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES)?
PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES) is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Behn Meyer & Co. (M) Sdn Bhd. The 510(k) number is K892030.
When did PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES) received FDA 510(k) clearance on 1989-05-01, under 510(k) number K892030.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES)?
The FDA 510(k) record lists Behn Meyer & Co. (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES)?
The FDA product code for PATIENT EXAM GLOVES (MFG. TAN CHONG RUBBER GLOVES) 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 Behn Meyer & Co. (M) Sdn 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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