N.I.T., INC. NEEDLE GUIDING TEMPLATE— 510(k) K973638
Substantially EquivalentAvid N.I.T., Inc.
FDA 510(k) clearance K973638 for N.I.T., INC. NEEDLE GUIDING TEMPLATE, Substantially Equivalent on 1997-12-23. Applicant: Avid N.I.T., Inc.. Device class: 1.
Clearance details
- Applicant
- Avid N.I.T., Inc.
- Product code
- Code IWJ
- Device class
- Class 1
- Regulation
- 21 CFR 892.5650
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Oldsmar, FL, US
Recent devices under product code IWJ
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- K983218 — N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLE
- K972595 — ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER
- K971645 — REGANES SPINAL NEEDLE (VARIOUS)
Data sourced from openFDA. This site is unofficial and independent of the FDA.