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)

NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33

K-Number: K992006 · 1999-08-17

ApplicantIntegra Neurocare, LLC
Decision Date1999-08-17
Product CodeOCV
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 is the device name listed in this FDA 510(k) record. The listed applicant is Integra Neurocare, LLC. It received FDA 510(k) clearance on 1999-08-17 under 510(k) number K992006. The device is classified under product code OCV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33?

NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 is a medical device that received FDA 510(k) clearance on 1999-08-17. The listed applicant is Integra Neurocare, LLC. The 510(k) number is K992006.

When did NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 receive FDA 510(k) clearance?

NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 received FDA 510(k) clearance on 1999-08-17, under 510(k) number K992006.

Who is the listed applicant for NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33?

The FDA 510(k) record lists Integra Neurocare, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33?

The FDA product code for NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 is OCV.

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 Integra Neurocare, LLC 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.

K002392VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-VK981246BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730)K973525MAURICE WORLDWIDE SHUNT SYSTEMK972994EXTERNAL CSF DRAINAGE MANAGEMENT SYSTEMSK972261RIVETTI-LEVINSON INSTRALUMINAL SHUNTK971617ENDOSCOPIC VENTRICULAR CATHETER

View all 12 devices →

Related Devices (Code: OCV)

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.

K240506KARL STORZ HoldersKarl Storz Endoscopy America, Inc.K232405ENDOFIX EXOAktormed GmbHK190576WalterLorenz Surgical Assist Arm Scope HolderBiomet MicrofixationK102179ENVIEW (TM)Carefusion 2200K093616V. MUELLER CAMERA CONTROLLER WITH STORAGE CARTCarefusion 2200K990334KSEA ENDOSCOPE HOLDERKARL STORZ Endoscopy-America, 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.

↑