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FDA 510(k)

KLEARTEX LATEX SURGICAL GLOVES

K-Number: K903069 · 1990-08-07

ApplicantTranscorp
Decision Date1990-08-07
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KLEARTEX LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Transcorp. It received FDA 510(k) clearance on 1990-08-07 under 510(k) number K903069. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLEARTEX LATEX SURGICAL GLOVES?

KLEARTEX LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1990-08-07. The listed applicant is Transcorp. The 510(k) number is K903069.

When did KLEARTEX LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

KLEARTEX LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1990-08-07, under 510(k) number K903069.

Who is the listed applicant for KLEARTEX LATEX SURGICAL GLOVES?

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

What is the FDA product code for KLEARTEX LATEX SURGICAL GLOVES?

The FDA product code for KLEARTEX LATEX SURGICAL GLOVES is KGO.

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 Transcorp 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: KGO)

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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