FDA 510(k)

HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE

K-Number: K942758 · 1994-07-08

Decision Date1994-07-08

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM 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 1994-07-08 under 510(k) number K942758. 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 HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE?

HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE is a medical device that received FDA 510(k) clearance on 1994-07-08. The listed applicant is Aladan Corp.. The 510(k) number is K942758.

When did HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE receive FDA 510(k) clearance?

HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE received FDA 510(k) clearance on 1994-07-08, under 510(k) number K942758.

Who is the listed applicant for HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM 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 HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE?

The FDA product code for HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE 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 K951839ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES K943883SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM

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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.