NOVA Lite DAPI ANA Kit
FDA 510(k) K150155 · Inova Diagnostics, Inc.
510(k) numberK150155
Submission
- Device name
- NOVA Lite DAPI ANA Kit
- Applicant
- Inova Diagnostics, Inc.
San Diego, CA, US - Received
- January 23, 2015
- Decision date
- April 8, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DHN – Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.5100
- Specialty
- Immunology
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Questions and answers
When was NOVA Lite DAPI ANA Kit cleared by the FDA?
NOVA Lite DAPI ANA Kit (K150155) received a 510(k) decision of Substantially Equivalent on April 8, 2015, 75 days after the submission was received.
What is the product code of K150155?
The FDA product code is DHN – Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.