AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN)
K-Number: K963866 · 1997-02-10
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Device Summary
Frequently Asked Questions
What is the AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN)?
AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN) is a medical device that received FDA 510(k) clearance on 1997-02-10. The listed applicant is Supertex Industrial, S.A. DE C.V.. The 510(k) number is K963866.
When did AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN) receive FDA 510(k) clearance?
AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN) received FDA 510(k) clearance on 1997-02-10, under 510(k) number K963866.
Who is the listed applicant for AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN)?
The FDA 510(k) record lists Supertex Industrial, S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN)?
The FDA product code for AMBIDERM (WHITE POW LATEX EXAM GLOVES W/ PROTEIN) 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 Supertex Industrial, S.A. DE C.V. 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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