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FDA 510(k)

PLASTIC TUBING CONNECTOR

K-Number: K874360 · 1987-11-17

ApplicantAmerican Medical Technology, Inc.
Decision Date1987-11-17
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC TUBING CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Technology, Inc.. It received FDA 510(k) clearance on 1987-11-17 under 510(k) number K874360. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC TUBING CONNECTOR?

PLASTIC TUBING CONNECTOR is a medical device that received FDA 510(k) clearance on 1987-11-17. The listed applicant is American Medical Technology, Inc.. The 510(k) number is K874360.

When did PLASTIC TUBING CONNECTOR receive FDA 510(k) clearance?

PLASTIC TUBING CONNECTOR received FDA 510(k) clearance on 1987-11-17, under 510(k) number K874360.

Who is the listed applicant for PLASTIC TUBING CONNECTOR?

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

What is the FDA product code for PLASTIC TUBING CONNECTOR?

The FDA product code for PLASTIC TUBING CONNECTOR is FPK.

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 American Medical Technology, 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.

K963808CHOICE POWERED WHEELCHAIRK905745AMETEC MASY MODULAR ANGIOSCOPE SYSTEMK874567RESUSCITATORK874430NEEDLE CONTAINERK873313SURGICAL DRAPE

Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, Inc.

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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