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FDA 510(k)

PERCUTANEOUS CATHETER INTRODUCER ADAPTER

K-Number: K800621 · 1980-04-24

Decision Date1980-04-24
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS CATHETER INTRODUCER ADAPTER 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 1980-04-24 under 510(k) number K800621. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUTANEOUS CATHETER INTRODUCER ADAPTER?

PERCUTANEOUS CATHETER INTRODUCER ADAPTER is a medical device that received FDA 510(k) clearance on 1980-04-24. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K800621.

When did PERCUTANEOUS CATHETER INTRODUCER ADAPTER receive FDA 510(k) clearance?

PERCUTANEOUS CATHETER INTRODUCER ADAPTER received FDA 510(k) clearance on 1980-04-24, under 510(k) number K800621.

Who is the listed applicant for PERCUTANEOUS CATHETER INTRODUCER ADAPTER?

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 PERCUTANEOUS CATHETER INTRODUCER ADAPTER?

The FDA product code for PERCUTANEOUS CATHETER INTRODUCER ADAPTER is DYB.

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.

Other records listing Norton Performance Plastics 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.

View all 39 devices →

Related Devices (Code: DYB)

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.

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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