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FDA 510(k)

NON-STERILE LATEX DENTAL PROCEDURE GLOVES

K-Number: K903857 · 1990-10-29

Decision Date1990-10-29
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-STERILE LATEX DENTAL PROCEDURE GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Formtex Medical Sdn. Bhd.. It received FDA 510(k) clearance on 1990-10-29 under 510(k) number K903857. 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 NON-STERILE LATEX DENTAL PROCEDURE GLOVES?

NON-STERILE LATEX DENTAL PROCEDURE GLOVES is a medical device that received FDA 510(k) clearance on 1990-10-29. The listed applicant is Formtex Medical Sdn. Bhd.. The 510(k) number is K903857.

When did NON-STERILE LATEX DENTAL PROCEDURE GLOVES receive FDA 510(k) clearance?

NON-STERILE LATEX DENTAL PROCEDURE GLOVES received FDA 510(k) clearance on 1990-10-29, under 510(k) number K903857.

Who is the listed applicant for NON-STERILE LATEX DENTAL PROCEDURE GLOVES?

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

What is the FDA product code for NON-STERILE LATEX DENTAL PROCEDURE GLOVES?

The FDA product code for NON-STERILE LATEX DENTAL PROCEDURE GLOVES 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 Formtex Medical Sdn. Bhd. 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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