Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE

K-Number: K902565 · 1990-07-03

ApplicantAladan Corp.
Decision Date1990-07-03
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Aladan Corp.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K902565. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE?

ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Aladan Corp.. The 510(k) number is K902565.

When did ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE receive FDA 510(k) clearance?

ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE received FDA 510(k) clearance on 1990-07-03, under 510(k) number K902565.

Who is the listed applicant for ALADAN TRI-CLEAN 110 POWDERLESS LATEX 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 TRI-CLEAN 110 POWDERLESS LATEX GLOVE?

The FDA product code for ALADAN TRI-CLEAN 110 POWDERLESS LATEX 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.

View all 18 devices →

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.

↑