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FDA 510(k)

DURHAM; MIN BORE LUER LOCK EXTENSION SET

K-Number: K930406 · 1993-09-03

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

Device Summary

DURHAM; MIN BORE LUER LOCK EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical, Inc.. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K930406. 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; MIN BORE LUER LOCK EXTENSION SET?

DURHAM; MIN BORE LUER LOCK EXTENSION SET is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Intl. Medical, Inc.. The 510(k) number is K930406.

When did DURHAM; MIN BORE LUER LOCK EXTENSION SET receive FDA 510(k) clearance?

DURHAM; MIN BORE LUER LOCK EXTENSION SET received FDA 510(k) clearance on 1993-09-03, under 510(k) number K930406.

Who is the listed applicant for DURHAM; MIN BORE LUER LOCK EXTENSION SET?

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

What is the FDA product code for DURHAM; MIN BORE LUER LOCK EXTENSION SET?

The FDA product code for DURHAM; MIN BORE LUER LOCK EXTENSION SET is FPA.

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Other records listing Intl. Medical, 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.

K970507PEAK FLOW METERK943078HOT BIOPSY FORCEPSK940370AMERICAN CATHETER E.R.C.P. CANNULAK940335AMERICAN CATHETER POLY-SNAREK942068AMERICAN CATHETER SPHINCTEROTOMEK930410DURHAM; LUER LOCK EXTENSION SET

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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

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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