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FDA 510(k)

PROTEX LATEX EXAMINATION GLOVE

K-Number: K900790 · 1990-04-05

Decision Date1990-04-05
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROTEX LATEX EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Seyen Intl., Inc.. It received FDA 510(k) clearance on 1990-04-05 under 510(k) number K900790. 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 PROTEX LATEX EXAMINATION GLOVE?

PROTEX LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1990-04-05. The listed applicant is Seyen Intl., Inc.. The 510(k) number is K900790.

When did PROTEX LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

PROTEX LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1990-04-05, under 510(k) number K900790.

Who is the listed applicant for PROTEX LATEX EXAMINATION GLOVE?

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

What is the FDA product code for PROTEX LATEX EXAMINATION GLOVE?

The FDA product code for PROTEX LATEX EXAMINATION GLOVE 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 Seyen Intl., Inc. 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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