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FDA 510(k)

LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED

K-Number: K981600 · 1998-11-02

Decision Date1998-11-02
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is Young Innovations, LLC Dba Plak Smacker. It received FDA 510(k) clearance on 1998-11-02 under 510(k) number K981600. 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 LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED?

LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED is a medical device that received FDA 510(k) clearance on 1998-11-02. The listed applicant is Young Innovations, LLC Dba Plak Smacker. The 510(k) number is K981600.

When did LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED received FDA 510(k) clearance on 1998-11-02, under 510(k) number K981600.

Who is the listed applicant for LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED?

The FDA 510(k) record lists Young Innovations, LLC Dba Plak Smacker as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED?

The FDA product code for LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED 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 Young Innovations, LLC Dba Plak Smacker 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

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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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