Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE STOPCOCKS

K-Number: K842173 · 1984-09-05

ApplicantProcedure Products, Inc.
Decision Date1984-09-05
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE STOPCOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Products, Inc.. It received FDA 510(k) clearance on 1984-09-05 under 510(k) number K842173. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE STOPCOCKS?

DISPOSABLE STOPCOCKS is a medical device that received FDA 510(k) clearance on 1984-09-05. The listed applicant is Procedure Products, Inc.. The 510(k) number is K842173.

When did DISPOSABLE STOPCOCKS receive FDA 510(k) clearance?

DISPOSABLE STOPCOCKS received FDA 510(k) clearance on 1984-09-05, under 510(k) number K842173.

Who is the listed applicant for DISPOSABLE STOPCOCKS?

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

What is the FDA product code for DISPOSABLE STOPCOCKS?

The FDA product code for DISPOSABLE STOPCOCKS is FMG.

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 Procedure 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.

K161812Freedom SyringeK923194INSUFFLATOR CONNECTING FILTERK922536TORQUE DEVICEK914128CONNECTING SETK910673BAG SPIGOTK884985MODIFIED 10CC SYRINGE CONTROL RING SET

View all 16 devices →

Related Devices (Code: FMG)

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.

K242255Qitexio® 4-Way Stopcock (QIT014)MedexK223499Three Way Stop CockM/S Romsons InternationalK223175lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare CorporationK211204SafePort(TM) Manifold (or Stopcock)Elcam Medical AcalK210516Clicky CrossYomura Technologies, Inc.K190539TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non SterileMonumedical, LLC

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.

↑