Mini Stick ENVI Non-Vascular Introducer Kit
FDA 510(k) K170775 · AngioDynamics, Inc.
510(k) numberK170775
Submission
- Device name
- Mini Stick ENVI Non-Vascular Introducer Kit
- Applicant
- AngioDynamics, Inc.
Marlborough, MA, US - Received
- March 14, 2017
- Decision date
- July 19, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DYB – Introducer, Catheter
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1340
- Specialty
- Cardiovascular
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Questions and answers
When was Mini Stick ENVI Non-Vascular Introducer Kit cleared by the FDA?
Mini Stick ENVI Non-Vascular Introducer Kit (K170775) received a 510(k) decision of Substantially Equivalent on July 19, 2017, 127 days after the submission was received.
What is the product code of K170775?
The FDA product code is DYB – Introducer, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1340.