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FDA 510(k)

MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE

K-Number: K902016 · 1990-05-16

ApplicantAor-Sullivan
Decision Date1990-05-16
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Aor-Sullivan. It received FDA 510(k) clearance on 1990-05-16 under 510(k) number K902016. 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 MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE?

MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE is a medical device that received FDA 510(k) clearance on 1990-05-16. The listed applicant is Aor-Sullivan. The 510(k) number is K902016.

When did MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE receive FDA 510(k) clearance?

MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE received FDA 510(k) clearance on 1990-05-16, under 510(k) number K902016.

Who is the listed applicant for MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE?

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

What is the FDA product code for MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE?

The FDA product code for MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE is LYU.

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.

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Other records listing Aor-Sullivan 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.

K893118AOR-SULLIVAN PROTECTIVE OVERGLOVE

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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