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)

CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET

K-Number: K052954 · 2006-02-15

ApplicantLife-Tech, Inc.
Decision Date2006-02-15
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech, Inc.. It received FDA 510(k) clearance on 2006-02-15 under 510(k) number K052954. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET?

CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET is a medical device that received FDA 510(k) clearance on 2006-02-15. The listed applicant is Life-Tech, Inc.. The 510(k) number is K052954.

When did CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET receive FDA 510(k) clearance?

CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET received FDA 510(k) clearance on 2006-02-15, under 510(k) number K052954.

Who is the listed applicant for CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET?

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

What is the FDA product code for CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET?

The FDA product code for CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET is CAZ.

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 Life-Tech, 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.

K120234EZONO 3000K111355ECHOBRIGHTK102813EZONO 3000K102007PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,K093662ECHOBRIGHTK093485VESISCAN

View all 14 devices →

Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK 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.

↑