PROGUIDE NEEDLE SET— 510(k) K060349
Substantially EquivalentNucletron Corporation
FDA 510(k) clearance K060349 for PROGUIDE NEEDLE SET, Substantially Equivalent on 2006-03-10. Applicant: Nucletron Corporation. Device class: 2.
Clearance details
- Applicant
- Nucletron Corporation
- Product code
- Code JAQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Columbia, MD, US
Recent devices under product code JAQ
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- K082642 — ONCENTRA RT VIEWER 1.0
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Data sourced from openFDA. This site is unofficial and independent of the FDA.