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FDA 510(k)

ALTERNATE STERILIZ. FOR CELLULOSE ACET

K-Number: K810315 · 1981-03-20

ApplicantCordis Corp.
Decision Date1981-03-20
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ALTERNATE STERILIZ. FOR CELLULOSE ACET is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810315. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTERNATE STERILIZ. FOR CELLULOSE ACET?

ALTERNATE STERILIZ. FOR CELLULOSE ACET is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Cordis Corp.. The 510(k) number is K810315.

When did ALTERNATE STERILIZ. FOR CELLULOSE ACET receive FDA 510(k) clearance?

ALTERNATE STERILIZ. FOR CELLULOSE ACET received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810315.

Who is the listed applicant for ALTERNATE STERILIZ. FOR CELLULOSE ACET?

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 ALTERNATE STERILIZ. FOR CELLULOSE ACET?

The FDA product code for ALTERNATE STERILIZ. FOR CELLULOSE ACET is FKQ.

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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: FKQ)

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.

K052764DIACAP ULTRA DIALYSIS FLUID FILTERB. Braun Medizintechnologie GmbHK893612TWO TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., Inc.K874084MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDMNational Medical Care, Medical Products Div., Inc.K873421KAWASUMI A.V. FISTULA SETKawasumi Laboratories Co., Ltd.K870889ACID FUCHSIN SOLUTIONSD.R.G. Scientific IndustriesK861730ACTRIL FOR KIDNEY MACHINE DISINFECTANTRenal Systems, 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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