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)

CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE

K-Number: K121846 · 2012-11-20

ApplicantB.Braun Medical, Inc.
Decision Date2012-11-20
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2012-11-20 under 510(k) number K121846. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE?

CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE is a medical device that received FDA 510(k) clearance on 2012-11-20. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K121846.

When did CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE receive FDA 510(k) clearance?

CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE received FDA 510(k) clearance on 2012-11-20, under 510(k) number K121846.

Who is the listed applicant for CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE?

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

What is the FDA product code for CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE?

The FDA product code for CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE is BSP.

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 B.Braun Medical, 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.

K254111Irrigation/Urology SetsK253235Introcan Safety® Deep Access XL IV CatheterK243392Infusomat® Space Volumetric Infusion Pump Administration SetsK240578VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter SystemK241845Introcan Safety® 2 IV CatheterK241385Omnifix Syringe NRFit

View all 142 devices →

Related Devices (Code: BSP)

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.

K243690SonoMSKPAJUNK GmbH MedizintechnologieK243682SonoPlex STIM; SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PuncturePAJUNK GmbH MedizintechnologieK243525SonoTAP and SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyPAJUNK GmbH MedizintechnologieK241954SonoBlock; SonoBlock IIPAJUNK GmbH Medizintechnologie

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.

↑