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FDA 510(k)

MONITORING LINES & FLUID ADMIN.

K-Number: K771387 · 1977-08-22

ApplicantNorton Performance Plastics Corp.
Decision Date1977-08-22
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONITORING LINES & FLUID ADMIN. 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 1977-08-22 under 510(k) number K771387. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITORING LINES & FLUID ADMIN.?

MONITORING LINES & FLUID ADMIN. is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K771387.

When did MONITORING LINES & FLUID ADMIN. receive FDA 510(k) clearance?

MONITORING LINES & FLUID ADMIN. received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771387.

Who is the listed applicant for MONITORING LINES & FLUID ADMIN.?

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 MONITORING LINES & FLUID ADMIN.?

The FDA product code for MONITORING LINES & FLUID ADMIN. is FPK.

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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: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, 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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