FDA 510(k)

CONTINUOUS FLUSH DEVICE, CAT. #14-370

K-Number: K791890 · 1979-12-13

ApplicantNorton Performance Plastics Corp.

Decision Date1979-12-13

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONTINUOUS FLUSH DEVICE, CAT. #14-370 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 1979-12-13 under 510(k) number K791890. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS FLUSH DEVICE, CAT. #14-370?

CONTINUOUS FLUSH DEVICE, CAT. #14-370 is a medical device that received FDA 510(k) clearance on 1979-12-13. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K791890.

When did CONTINUOUS FLUSH DEVICE, CAT. #14-370 receive FDA 510(k) clearance?

CONTINUOUS FLUSH DEVICE, CAT. #14-370 received FDA 510(k) clearance on 1979-12-13, under 510(k) number K791890.

Who is the listed applicant for CONTINUOUS FLUSH DEVICE, CAT. #14-370?

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 CONTINUOUS FLUSH DEVICE, CAT. #14-370?

The FDA product code for CONTINUOUS FLUSH DEVICE, CAT. #14-370 is KRA.

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Other records listing Norton Performance Plastics Corp. as applicant

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Related Devices (Code: KRA)

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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.