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FDA 510(k)

I.V. SET WITH IN-LINE FILTER

K-Number: K781785 · 1978-12-07

ApplicantCutler Laboratories, Inc.
Decision Date1978-12-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. SET WITH IN-LINE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Cutler Laboratories, Inc.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781785. 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 I.V. SET WITH IN-LINE FILTER?

I.V. SET WITH IN-LINE FILTER is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Cutler Laboratories, Inc.. The 510(k) number is K781785.

When did I.V. SET WITH IN-LINE FILTER receive FDA 510(k) clearance?

I.V. SET WITH IN-LINE FILTER received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781785.

Who is the listed applicant for I.V. SET WITH IN-LINE FILTER?

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

What is the FDA product code for I.V. SET WITH IN-LINE FILTER?

The FDA product code for I.V. SET WITH IN-LINE FILTER is FPA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cutler Laboratories, 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.

K781140CUTTER RESIFLEX FOLEY CATHETERS

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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