NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES— 510(k) K962319
Substantially EquivalentNeoprobe Corp.
FDA 510(k) clearance K962319 for NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES, Substantially Equivalent on 1996-09-13. Applicant: Neoprobe Corp.. Device class: 1.
Clearance details
- Applicant
- Neoprobe Corp.
- Product code
- Code IZD
- Device class
- Class 1
- Regulation
- 21 CFR 892.1320
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dublin, OH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.