MODIFIED STERILE LATEX EXAMINATION GLOVES
K-Number: K902182 · 1990-06-01
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Device Summary
Frequently Asked Questions
What is the MODIFIED STERILE LATEX EXAMINATION GLOVES?
MODIFIED STERILE LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-06-01. The listed applicant is Aladan Corp.. The 510(k) number is K902182.
When did MODIFIED STERILE LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
MODIFIED STERILE LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1990-06-01, under 510(k) number K902182.
Who is the listed applicant for MODIFIED STERILE LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Aladan Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED STERILE LATEX EXAMINATION GLOVES?
The FDA product code for MODIFIED STERILE LATEX EXAMINATION GLOVES 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 Aladan 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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