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FDA 510(k)

PROTECTIVE LATEX POWDERED GLOVES

K-Number: K960277 · 1996-05-15

ApplicantHighactive Sdn. Bhd.
Decision Date1996-05-15
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROTECTIVE LATEX POWDERED GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Highactive Sdn. Bhd.. It received FDA 510(k) clearance on 1996-05-15 under 510(k) number K960277. 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 PROTECTIVE LATEX POWDERED GLOVES?

PROTECTIVE LATEX POWDERED GLOVES is a medical device that received FDA 510(k) clearance on 1996-05-15. The listed applicant is Highactive Sdn. Bhd.. The 510(k) number is K960277.

When did PROTECTIVE LATEX POWDERED GLOVES receive FDA 510(k) clearance?

PROTECTIVE LATEX POWDERED GLOVES received FDA 510(k) clearance on 1996-05-15, under 510(k) number K960277.

Who is the listed applicant for PROTECTIVE LATEX POWDERED GLOVES?

The FDA 510(k) record lists Highactive Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTECTIVE LATEX POWDERED GLOVES?

The FDA product code for PROTECTIVE LATEX POWDERED GLOVES is LYY.

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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.

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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.

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