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FDA 510(k)

NYLON LINER GLOVES

K-Number: K940274 · 1994-05-12

ApplicantWells Lamont Corp.
Decision Date1994-05-12
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NYLON LINER GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Wells Lamont Corp.. It received FDA 510(k) clearance on 1994-05-12 under 510(k) number K940274. 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 NYLON LINER GLOVES?

NYLON LINER GLOVES is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Wells Lamont Corp.. The 510(k) number is K940274.

When did NYLON LINER GLOVES receive FDA 510(k) clearance?

NYLON LINER GLOVES received FDA 510(k) clearance on 1994-05-12, under 510(k) number K940274.

Who is the listed applicant for NYLON LINER GLOVES?

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

What is the FDA product code for NYLON LINER GLOVES?

The FDA product code for NYLON LINER GLOVES 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 Wells Lamont 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.

K944763CUT-TEC OR WELLS LAMONT POLYESTER/WIRE CUT-RESISTANT GLOVE LINER WELLS-TEC, SCEPTERK925937WELLS LAMONT HANDAGES/MED WRAP DRESSINGSK922407WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS

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

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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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