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)

TRU-SWAB STOCOCK

K-Number: K052330 · 2005-09-09

ApplicantMedegen Medical Manufacturing Services
Decision Date2005-09-09
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRU-SWAB STOCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Medegen Medical Manufacturing Services. It received FDA 510(k) clearance on 2005-09-09 under 510(k) number K052330. 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 TRU-SWAB STOCOCK?

TRU-SWAB STOCOCK is a medical device that received FDA 510(k) clearance on 2005-09-09. The listed applicant is Medegen Medical Manufacturing Services. The 510(k) number is K052330.

When did TRU-SWAB STOCOCK receive FDA 510(k) clearance?

TRU-SWAB STOCOCK received FDA 510(k) clearance on 2005-09-09, under 510(k) number K052330.

Who is the listed applicant for TRU-SWAB STOCOCK?

The FDA 510(k) record lists Medegen Medical Manufacturing Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRU-SWAB STOCOCK?

The FDA product code for TRU-SWAB STOCOCK 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 Medegen Medical Manufacturing Services 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.

K083765MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIALK051930DRUG ACCESS SPIKEK051499INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET

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.

↑