BG PATIENT EXAMINATION GLOVES, NON-STERILE
K-Number: K961675 · 1996-07-25
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Device Summary
Frequently Asked Questions
What is the BG PATIENT EXAMINATION GLOVES, NON-STERILE?
BG PATIENT EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Biografik (Malaysia) Sdn Bhd. The 510(k) number is K961675.
When did BG PATIENT EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?
BG PATIENT EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961675.
Who is the listed applicant for BG PATIENT EXAMINATION GLOVES, NON-STERILE?
The FDA 510(k) record lists Biografik (Malaysia) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BG PATIENT EXAMINATION GLOVES, NON-STERILE?
The FDA product code for BG PATIENT EXAMINATION GLOVES, NON-STERILE 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 Biografik (Malaysia) 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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