PROTEX PATIENT EXAMINATION GLOVES (LATEX)
K-Number: K892115 · 1989-04-25
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Device Summary
Frequently Asked Questions
What is the PROTEX PATIENT EXAMINATION GLOVES (LATEX)?
PROTEX PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Pt Nusa Dipa Perdana. The 510(k) number is K892115.
When did PROTEX PATIENT EXAMINATION GLOVES (LATEX) receive FDA 510(k) clearance?
PROTEX PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-04-25, under 510(k) number K892115.
Who is the listed applicant for PROTEX PATIENT EXAMINATION GLOVES (LATEX)?
The FDA 510(k) record lists Pt Nusa Dipa Perdana as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEX PATIENT EXAMINATION GLOVES (LATEX)?
The FDA product code for PROTEX PATIENT EXAMINATION 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.
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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