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FDA 510(k)

INTRAVENOUS FILTER SET

K-Number: K834130 · 1984-01-30

ApplicantTri-Med, Inc.
Decision Date1984-01-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS FILTER SET is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med, Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834130. 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 INTRAVENOUS FILTER SET?

INTRAVENOUS FILTER SET is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Tri-Med, Inc.. The 510(k) number is K834130.

When did INTRAVENOUS FILTER SET receive FDA 510(k) clearance?

INTRAVENOUS FILTER SET received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834130.

Who is the listed applicant for INTRAVENOUS FILTER SET?

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

What is the FDA product code for INTRAVENOUS FILTER SET?

The FDA product code for INTRAVENOUS FILTER SET is FPA.

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Other records listing Tri-Med, 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.

K040112TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATEK030877TRIMED RADIAL BULLETK010545TBWK961863PARACENTESIS TRAYSK875224HUDSON CRANINAL BURRSK850747TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR

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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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