NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33— 510(k) K992006
Substantially EquivalentIntegra Neurocare, LLC
FDA 510(k) clearance K992006 for NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33, Substantially Equivalent on 1999-08-17. Applicant: Integra Neurocare, LLC. Device class: 2.
Clearance details
- Applicant
- Integra Neurocare, LLC
- Product code
- Code OCV
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.