STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC
K-Number: K924959 · 1993-03-03
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Device Summary
Frequently Asked Questions
What is the STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC?
STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC is a medical device that received FDA 510(k) clearance on 1993-03-03. The listed applicant is Perlink USA, Inc.. The 510(k) number is K924959.
When did STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC receive FDA 510(k) clearance?
STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC received FDA 510(k) clearance on 1993-03-03, under 510(k) number K924959.
Who is the listed applicant for STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC?
The FDA 510(k) record lists Perlink USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC?
The FDA product code for STERLING LATEX EXAM GLOVE, HYPO-ALLERGENIC 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 Perlink USA, Inc. 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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