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FDA 510(k)

DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK

K-Number: K930974 · 1993-11-03

ApplicantIntl. Medical Consultants
Decision Date1993-11-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK 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 1993-11-03 under 510(k) number K930974. 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; INJECTION SITE EXTENSION SET, LUER LOCK?

DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Intl. Medical Consultants. The 510(k) number is K930974.

When did DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK receive FDA 510(k) clearance?

DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK received FDA 510(k) clearance on 1993-11-03, under 510(k) number K930974.

Who is the listed applicant for DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK?

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; INJECTION SITE EXTENSION SET, LUER LOCK?

The FDA product code for DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK is FPA.

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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.

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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 SETK930926DURHAM; Y CHECK SET-LUER LOCK W/INJECTION SITEK930751DURHAM; EXTENSION TUBE 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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