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FDA 510(k)

MODIFICATION TO MALE TO MALE LUER ADAPTER

K-Number: K003712 · 2001-05-16

ApplicantMolded Products, Inc.
Decision Date2001-05-16
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MALE TO MALE LUER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Molded Products, Inc.. It received FDA 510(k) clearance on 2001-05-16 under 510(k) number K003712. 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 MODIFICATION TO MALE TO MALE LUER ADAPTER?

MODIFICATION TO MALE TO MALE LUER ADAPTER is a medical device that received FDA 510(k) clearance on 2001-05-16. The listed applicant is Molded Products, Inc.. The 510(k) number is K003712.

When did MODIFICATION TO MALE TO MALE LUER ADAPTER receive FDA 510(k) clearance?

MODIFICATION TO MALE TO MALE LUER ADAPTER received FDA 510(k) clearance on 2001-05-16, under 510(k) number K003712.

Who is the listed applicant for MODIFICATION TO MALE TO MALE LUER ADAPTER?

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

What is the FDA product code for MODIFICATION TO MALE TO MALE LUER ADAPTER?

The FDA product code for MODIFICATION TO MALE TO MALE LUER ADAPTER is KOC.

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Other records listing Molded Products, 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.

K022068TUBING, DIALYSATE (AND CONNECTOR)K010366DISPOSABLE STORAGE CAPK010712DIALYSATE LINE WITH CONNECTORS/RE-USE WASH-OUT LINESK925978MPC-80 TRANSDUCERK925927MPC-1000 INJECTION CAP/PLUGK925930MPC-150 MALE TO MALE LUER ADAPTER

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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.

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.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.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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