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FDA 510(k)

STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV

K-Number: K923589 · 1993-07-23

Decision Date1993-07-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV is the device name listed in this FDA 510(k) record. The listed applicant is Tomarc (M) Sdn Bhd. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K923589. 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 STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV?

STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Tomarc (M) Sdn Bhd. The 510(k) number is K923589.

When did STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV receive FDA 510(k) clearance?

STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV received FDA 510(k) clearance on 1993-07-23, under 510(k) number K923589.

Who is the listed applicant for STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV?

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

What is the FDA product code for STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV?

The FDA product code for STERILE HYPOALLERGENIC POWDER-FREE LATEX SURG. GLV 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 Tomarc (M) 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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