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FDA 510(k)

TRITON MEIDCAL TMED IV-SET

K-Number: K073444 · 2008-08-18

ApplicantTriton Medical, LLC
Decision Date2008-08-18
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRITON MEIDCAL TMED IV-SET is the device name listed in this FDA 510(k) record. The listed applicant is Triton Medical, LLC. It received FDA 510(k) clearance on 2008-08-18 under 510(k) number K073444. 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 TRITON MEIDCAL TMED IV-SET?

TRITON MEIDCAL TMED IV-SET is a medical device that received FDA 510(k) clearance on 2008-08-18. The listed applicant is Triton Medical, LLC. The 510(k) number is K073444.

When did TRITON MEIDCAL TMED IV-SET receive FDA 510(k) clearance?

TRITON MEIDCAL TMED IV-SET received FDA 510(k) clearance on 2008-08-18, under 510(k) number K073444.

Who is the listed applicant for TRITON MEIDCAL TMED IV-SET?

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

What is the FDA product code for TRITON MEIDCAL TMED IV-SET?

The FDA product code for TRITON MEIDCAL TMED IV-SET is FPA.

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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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