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FDA 510(k)

TOUCH FLUSH W/Y TRANSDUCER CONNECTOR

K-Number: K820676 · 1982-03-25

ApplicantNorton Performance Plastics Corp.
Decision Date1982-03-25
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TOUCH FLUSH W/Y TRANSDUCER CONNECTOR 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 1982-03-25 under 510(k) number K820676. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOUCH FLUSH W/Y TRANSDUCER CONNECTOR?

TOUCH FLUSH W/Y TRANSDUCER CONNECTOR is a medical device that received FDA 510(k) clearance on 1982-03-25. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K820676.

When did TOUCH FLUSH W/Y TRANSDUCER CONNECTOR receive FDA 510(k) clearance?

TOUCH FLUSH W/Y TRANSDUCER CONNECTOR received FDA 510(k) clearance on 1982-03-25, under 510(k) number K820676.

Who is the listed applicant for TOUCH FLUSH W/Y TRANSDUCER CONNECTOR?

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 TOUCH FLUSH W/Y TRANSDUCER CONNECTOR?

The FDA product code for TOUCH FLUSH W/Y TRANSDUCER CONNECTOR is DRS.

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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: DRS)

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.

K254074TruPressProcerus EnterprisesK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsEdwards Lifesciences, LLCK221782Meritrans ECO Reusable Pressure Transducer, Meritrans ECO DomesMerit Medical Pte. , Ltd.K172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K161408Compass Cast and MAPCenturion Medical Products Corporation

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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