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FDA 510(k)

DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE

K-Number: K930751 · 1993-09-03

ApplicantIntl. Medical Consultants
Decision Date1993-09-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Consultants. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K930751. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE?

DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Intl. Medical Consultants. The 510(k) number is K930751.

When did DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE receive FDA 510(k) clearance?

DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE received FDA 510(k) clearance on 1993-09-03, under 510(k) number K930751.

Who is the listed applicant for DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE?

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

What is the FDA product code for DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE?

The FDA product code for DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE is FPA.

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Other records listing Intl. Medical Consultants 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.

K930927DURHAM;T ADAPTOR EXTENSIONSET W/INJECTION SITEK931119DURHAM; NON CORING WINGED ADMINISTRATION SETK930974DURHAM; INJECTION SITE EXTENSION SET, LUER LOCKK930926DURHAM; Y CHECK SET-LUER LOCK W/INJECTION SITEK930750DURHAM; ADM. SET-LUER LOCK W/.22 MICRON FILTER

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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