FDA 510(k)

PERM. REPAIR KIT FOR LEONARD NORTON DUAL

K-Number: K830969 · 1983-04-14

ApplicantNorton Performance Plastics Corp.

Decision Date1983-04-14

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PERM. REPAIR KIT FOR LEONARD NORTON DUAL is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1983-04-14 under 510(k) number K830969. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERM. REPAIR KIT FOR LEONARD NORTON DUAL?

PERM. REPAIR KIT FOR LEONARD NORTON DUAL is a medical device that received FDA 510(k) clearance on 1983-04-14. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K830969.

When did PERM. REPAIR KIT FOR LEONARD NORTON DUAL receive FDA 510(k) clearance?

PERM. REPAIR KIT FOR LEONARD NORTON DUAL received FDA 510(k) clearance on 1983-04-14, under 510(k) number K830969.

Who is the listed applicant for PERM. REPAIR KIT FOR LEONARD NORTON DUAL?

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

What is the FDA product code for PERM. REPAIR KIT FOR LEONARD NORTON DUAL?

The FDA product code for PERM. REPAIR KIT FOR LEONARD NORTON DUAL is LJS.

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Other records listing Norton Performance Plastics Corp. as applicant

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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.