POWDER-FREE LATEX EXAMINATION GLOVE
K-Number: K934546 · 1994-01-07
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE LATEX EXAMINATION GLOVE?
POWDER-FREE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Powercrest (M) Sdn. Bhd.. The 510(k) number is K934546.
When did POWDER-FREE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER-FREE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1994-01-07, under 510(k) number K934546.
Who is the listed applicant for POWDER-FREE LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Powercrest (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 GLOVE?
The FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE 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 Powercrest (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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