POWDER FREE LATEX EXAMINATION GLOVES
K-Number: K935946 · 1994-06-21
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Device Summary
Frequently Asked Questions
What is the POWDER FREE LATEX EXAMINATION GLOVES?
POWDER FREE LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1994-06-21. The listed applicant is Cranberry (M) Sdn. Bhd.. The 510(k) number is K935946.
When did POWDER FREE LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER FREE LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1994-06-21, under 510(k) number K935946.
Who is the listed applicant for POWDER FREE LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Cranberry (M) Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE LATEX EXAMINATION GLOVES?
The FDA product code for POWDER FREE 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 Cranberry (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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