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FDA 510(k)

NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER

K-Number: K910890 · 1991-06-27

ApplicantLovell-Schenck, Inc.
Decision Date1991-06-27
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER is the device name listed in this FDA 510(k) record. The listed applicant is Lovell-Schenck, Inc.. It received FDA 510(k) clearance on 1991-06-27 under 510(k) number K910890. 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 NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER?

NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER is a medical device that received FDA 510(k) clearance on 1991-06-27. The listed applicant is Lovell-Schenck, Inc.. The 510(k) number is K910890.

When did NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER receive FDA 510(k) clearance?

NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER received FDA 510(k) clearance on 1991-06-27, under 510(k) number K910890.

Who is the listed applicant for NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER?

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

What is the FDA product code for NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER?

The FDA product code for NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER is LYU.

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Other records listing Lovell-Schenck, 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.

K904903PARADERM(TM) SURGEON'S GLOVE ACCESSORY

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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