FDA 510(k)

CENTRAL VEIN CATHERIZATION KIT-14-690-

K-Number: K830788 · 1983-04-30

ApplicantNorton Performance Plastics Corp.

Decision Date1983-04-30

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CENTRAL VEIN CATHERIZATION KIT-14-690- 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 1983-04-30 under 510(k) number K830788. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VEIN CATHERIZATION KIT-14-690-?

CENTRAL VEIN CATHERIZATION KIT-14-690- is a medical device that received FDA 510(k) clearance on 1983-04-30. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K830788.

When did CENTRAL VEIN CATHERIZATION KIT-14-690- receive FDA 510(k) clearance?

CENTRAL VEIN CATHERIZATION KIT-14-690- received FDA 510(k) clearance on 1983-04-30, under 510(k) number K830788.

Who is the listed applicant for CENTRAL VEIN CATHERIZATION KIT-14-690-?

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 CENTRAL VEIN CATHERIZATION KIT-14-690-?

The FDA product code for CENTRAL VEIN CATHERIZATION KIT-14-690- is DQO.

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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.