ALADAN STERILE LATEX MEDICAL GLOVE
K-Number: K890880 · 1989-03-29
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Device Summary
Frequently Asked Questions
What is the ALADAN STERILE LATEX MEDICAL GLOVE?
ALADAN STERILE LATEX MEDICAL GLOVE is a medical device that received FDA 510(k) clearance on 1989-03-29. The listed applicant is Aladan Corp.. The 510(k) number is K890880.
When did ALADAN STERILE LATEX MEDICAL GLOVE receive FDA 510(k) clearance?
ALADAN STERILE LATEX MEDICAL GLOVE received FDA 510(k) clearance on 1989-03-29, under 510(k) number K890880.
Who is the listed applicant for ALADAN STERILE LATEX MEDICAL GLOVE?
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 ALADAN STERILE LATEX MEDICAL GLOVE?
The FDA product code for ALADAN STERILE LATEX MEDICAL GLOVE 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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