POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE
K-Number: K070760 · 2007-06-07
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Device Summary
Frequently Asked Questions
What is the POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE?
POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2007-06-07. The listed applicant is Derma Care Plus Products, LLC. The 510(k) number is K070760.
When did POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 2007-06-07, under 510(k) number K070760.
Who is the listed applicant for POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE?
The FDA 510(k) record lists Derma Care Plus Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE?
The FDA product code for POWDER FREE CHLORINATED LATEX PATIENT 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 Derma Care Plus Products, LLC 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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