OSTAR EXAMINATION GLOVES
K-Number: K955947 · 1996-06-10
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Device Summary
Frequently Asked Questions
What is the OSTAR EXAMINATION GLOVES?
OSTAR EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1996-06-10. The listed applicant is Contract Latex Dippers Sdn Bhd. The 510(k) number is K955947.
When did OSTAR EXAMINATION GLOVES receive FDA 510(k) clearance?
OSTAR EXAMINATION GLOVES received FDA 510(k) clearance on 1996-06-10, under 510(k) number K955947.
Who is the listed applicant for OSTAR EXAMINATION GLOVES?
The FDA 510(k) record lists Contract Latex Dippers Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTAR EXAMINATION GLOVES?
The FDA product code for OSTAR EXAMINATION 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 Contract Latex Dippers 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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