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FDA 510(k)

BLOOD TUBING SET

K-Number: K832103 · 1983-08-12

ApplicantLee Medical Intl., Inc.
Decision Date1983-08-12
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLOOD TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Lee Medical Intl., Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832103. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD TUBING SET?

BLOOD TUBING SET is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Lee Medical Intl., Inc.. The 510(k) number is K832103.

When did BLOOD TUBING SET receive FDA 510(k) clearance?

BLOOD TUBING SET received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832103.

Who is the listed applicant for BLOOD TUBING SET?

The FDA 510(k) record lists Lee Medical Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD TUBING SET?

The FDA product code for BLOOD TUBING SET is KOC.

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Other records listing Lee Medical Intl., Inc. 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.

K840082STERILE INSULIN DISPOS. NEEDLE/SYRINGEK840081IV ADMINISTRATION SETK840083STERILE INSULIN DISPOS. NEEDLE/GREENK832104STERILE DISP. BUTTERFLY INFUSION SETK832105ADMINISTRATIVE IV SETK832101STERILE DISPOSABLE SYRINGE

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Related Devices (Code: KOC)

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.

K242176BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series (AL-ADC-E(U), AL-CDC-E(U), C18RDC-E(U), C18BDD-E(U), C18SFD-E(U)NIKKISO CO., LTD.K242479BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series AL-ADC-PU, AL-CDC-PU, C18RDC-PU, C18BDD-PU, C18SFD-PUNIKKISO CO., LTD.K231589Blood Tubing Lines for Hemodialysis AV06C-ENIKKISO CO., LTD.K230514Blood Tubing Lines for Hemodialysis AL Series (Archloop), Blood Tubing Lines for Hemodialysis C18 SeriesNIKKISO CO., LTD.K201207CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Integrated Crit-Line Technology, CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Intergrated Crit-Line Technology, no Heparin LineFresenius Medical Care Renal Therapies Group, LLCK172238CAREline Airless Hemodialysis Blood Tubing SetsFresenius Medical Care Renal Therapies Group, LLC

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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