SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)
K-Number: K891854 · 1989-04-11
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Device Summary
Frequently Asked Questions
What is the SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)?
SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX) is a medical device that received FDA 510(k) clearance on 1989-04-11. The listed applicant is Unidus Corp.. The 510(k) number is K891854.
When did SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX) receive FDA 510(k) clearance?
SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX) received FDA 510(k) clearance on 1989-04-11, under 510(k) number K891854.
Who is the listed applicant for SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)?
The FDA 510(k) record lists Unidus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)?
The FDA product code for SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX) 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 Unidus Corp. 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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