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FDA 510(k)

CORDIS DOW SERA FLO TM TRANSDUCER PROT

K-Number: K811892 · 1981-07-31

ApplicantCordis Corp.
Decision Date1981-07-31
Product CodeFIB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORDIS DOW SERA FLO TM TRANSDUCER PROT is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1981-07-31 under 510(k) number K811892. The device is classified under product code FIB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS DOW SERA FLO TM TRANSDUCER PROT?

CORDIS DOW SERA FLO TM TRANSDUCER PROT is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Cordis Corp.. The 510(k) number is K811892.

When did CORDIS DOW SERA FLO TM TRANSDUCER PROT receive FDA 510(k) clearance?

CORDIS DOW SERA FLO TM TRANSDUCER PROT received FDA 510(k) clearance on 1981-07-31, under 510(k) number K811892.

Who is the listed applicant for CORDIS DOW SERA FLO TM TRANSDUCER PROT?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORDIS DOW SERA FLO TM TRANSDUCER PROT?

The FDA product code for CORDIS DOW SERA FLO TM TRANSDUCER PROT is FIB.

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Other records listing Cordis 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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Related Devices (Code: FIB)

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.

K240164NovaLine SP-C35 Transducer Protector (956007)Bain Medical Equipment (Guangzhou) Co., Ltd.K072988NIPRO TRANSDUCER PROTECTOR TP-SURE, MODEL TPSURE+1Nipro Medical CorporationK001971HEMODIALYSIS TUBING SETSOfi Biomedica S.P.A.K010264NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SETNipro Medical Corp.K001465NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SETNipro Medical Corp.K003445FRESENIUS VIRAL BLOCKING TRANSDUCER PROTECTOR FOR HEMODIALYSIS, MODEL 04-9500-2Fresenius Medical Care North America

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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