TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETS— 510(k) K080871
Substantially EquivalentNucletron Corporation
FDA 510(k) clearance K080871 for TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETS, Substantially Equivalent on 2008-04-29. 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.