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FDA 510(k)

PVC QUICK PRIME LINES

K-Number: K780984 · 1978-07-17

ApplicantNorton Performance Plastics Corp.
Decision Date1978-07-17
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PVC QUICK PRIME LINES 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 1978-07-17 under 510(k) number K780984. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVC QUICK PRIME LINES?

PVC QUICK PRIME LINES is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K780984.

When did PVC QUICK PRIME LINES receive FDA 510(k) clearance?

PVC QUICK PRIME LINES received FDA 510(k) clearance on 1978-07-17, under 510(k) number K780984.

Who is the listed applicant for PVC QUICK PRIME LINES?

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 PVC QUICK PRIME LINES?

The FDA product code for PVC QUICK PRIME LINES is KRI.

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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.

K853791NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000K852914ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSIONK851299CORRECT FLOK842858FLUID ADMINISTRATION LINE W/SPIKE 14-923K841828CENTRAL VENOUS CATHETER W/BIG-GARDK840240MICROFUSE INTRAVENOUS CATHETER SET

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Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, Inc.

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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