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FDA 510(k)

MAXCESS NEEDLE FREE CONNECTOR (8200)

K-Number: K960661 · 1996-03-21

ApplicantSolopak Medical Products, Inc.
Decision Date1996-03-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAXCESS NEEDLE FREE CONNECTOR (8200) is the device name listed in this FDA 510(k) record. The listed applicant is Solopak Medical Products, Inc.. It received FDA 510(k) clearance on 1996-03-21 under 510(k) number K960661. 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 MAXCESS NEEDLE FREE CONNECTOR (8200)?

MAXCESS NEEDLE FREE CONNECTOR (8200) is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Solopak Medical Products, Inc.. The 510(k) number is K960661.

When did MAXCESS NEEDLE FREE CONNECTOR (8200) receive FDA 510(k) clearance?

MAXCESS NEEDLE FREE CONNECTOR (8200) received FDA 510(k) clearance on 1996-03-21, under 510(k) number K960661.

Who is the listed applicant for MAXCESS NEEDLE FREE CONNECTOR (8200)?

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

What is the FDA product code for MAXCESS NEEDLE FREE CONNECTOR (8200)?

The FDA product code for MAXCESS NEEDLE FREE CONNECTOR (8200) 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 Solopak Medical Products, 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.

K970800MAXCESS NEEDLEFREE - Y- SITE (100713)K963355SOLOPAK PARAGON INFUSOR PUMP AND INFUSION SETK962663SOLOPAK SIDEKICK INFUSION PUMP AND ADMINISTATION 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

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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