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FDA 510(k)

CUSTOM TUBING SETS

K-Number: K790604 · 1979-05-04

Decision Date1979-05-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CUSTOM TUBING SETS 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 1979-05-04 under 510(k) number K790604. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSTOM TUBING SETS?

CUSTOM TUBING SETS is a medical device that received FDA 510(k) clearance on 1979-05-04. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K790604.

When did CUSTOM TUBING SETS receive FDA 510(k) clearance?

CUSTOM TUBING SETS received FDA 510(k) clearance on 1979-05-04, under 510(k) number K790604.

Who is the listed applicant for CUSTOM TUBING SETS?

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 CUSTOM TUBING SETS?

The FDA product code for CUSTOM TUBING SETS is FPA.

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: FPA)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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