FDA 510(k)

ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES

K-Number: K951839 · 1995-06-15

Decision Date1995-06-15

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Aladan Corp.. It received FDA 510(k) clearance on 1995-06-15 under 510(k) number K951839. 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 HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES?

ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1995-06-15. The listed applicant is Aladan Corp.. The 510(k) number is K951839.

When did ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES receive FDA 510(k) clearance?

ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES received FDA 510(k) clearance on 1995-06-15, under 510(k) number K951839.

Who is the listed applicant for ALADAN HYPOALLERGENIC LATEX MEDICAL 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 ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES?

The FDA product code for ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES is LYY.

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Other records listing Aladan Corp. as applicant

K960590TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE K952404SAFETEX SUPER HYPERALLERGENIC POWDERFREE LATEX MEDICAL GLOVE K952556SAFETEX SUPER HYPOALLERGENIC POWDERED LATEX EXAMINATION GLOVE K943933SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM K943883SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM K942758HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE

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Related Devices (Code: LYY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.