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FDA 510(k)

KIPP MED I.V. MANIFOLD

K-Number: K970255 · 1997-04-14

ApplicantThe Kipp Group
Decision Date1997-04-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KIPP MED I.V. MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is The Kipp Group. It received FDA 510(k) clearance on 1997-04-14 under 510(k) number K970255. 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 KIPP MED I.V. MANIFOLD?

KIPP MED I.V. MANIFOLD is a medical device that received FDA 510(k) clearance on 1997-04-14. The listed applicant is The Kipp Group. The 510(k) number is K970255.

When did KIPP MED I.V. MANIFOLD receive FDA 510(k) clearance?

KIPP MED I.V. MANIFOLD received FDA 510(k) clearance on 1997-04-14, under 510(k) number K970255.

Who is the listed applicant for KIPP MED I.V. MANIFOLD?

The FDA 510(k) record lists The Kipp Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIPP MED I.V. MANIFOLD?

The FDA product code for KIPP MED I.V. MANIFOLD 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 The Kipp Group 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.

K000343NAC Y-ADPK000152KIPPMED I.V. MANIFOLDK993147DECAPK992268NAC PRN NEEDLELESS ACCESS CONNECTORK991932INTRAVASCULAR ADMINISTRATION SET

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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