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FDA 510(k)

SURGICAL COTTON GLOVES

K-Number: K900425 · 1990-09-07

ApplicantAllo Pro Corp.
Decision Date1990-09-07
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL COTTON GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1990-09-07 under 510(k) number K900425. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL COTTON GLOVES?

SURGICAL COTTON GLOVES is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Allo Pro Corp.. The 510(k) number is K900425.

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

SURGICAL COTTON GLOVES received FDA 510(k) clearance on 1990-09-07, under 510(k) number K900425.

Who is the listed applicant for SURGICAL COTTON GLOVES?

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

What is the FDA product code for SURGICAL COTTON GLOVES?

The FDA product code for SURGICAL COTTON GLOVES is LYU.

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Other records listing Allo Pro Corp. 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.

K901581GSB ELBOWK900392CENTERING PLUGK896669WEBER PERMALOCKK892644BIOLOX CERAMIC BALLK885049RS-CUP ACETABULAR PROSTHESISK864999KENNEDY STEM

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Related Devices (Code: LYU)

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.

K011755STRYKER T4 HYTREL (R) TOGASStryker Corp.K965237NURSES BOUFFANT CAPCopioumed Intl., Inc.K970988FAR-EAST BOUFFANT CAPSFar East Science & Technology Development Co., Ltd.K964364DISPOSABLE APRONInstrument Makar, Inc.K961791DEPUY DISPOSABLE FILTER/HOODDepuy, Inc.K961454AMMI MAGNI-GUARDAmerican Medical Mfg., Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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