ACRYLIC DIPPED LATEX EXAMINATION GLOVES
K-Number: K945506 · 1995-10-12
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Device Summary
Frequently Asked Questions
What is the ACRYLIC DIPPED LATEX EXAMINATION GLOVES?
ACRYLIC DIPPED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is Ganz Industries Sdn. Bhd.. The 510(k) number is K945506.
When did ACRYLIC DIPPED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
ACRYLIC DIPPED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1995-10-12, under 510(k) number K945506.
Who is the listed applicant for ACRYLIC DIPPED LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Ganz Industries Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACRYLIC DIPPED LATEX EXAMINATION GLOVES?
The FDA product code for ACRYLIC DIPPED LATEX 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 Ganz Industries 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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