Modified Flowgate Balloon Guide Catheter
FDA 510(k) K131492 · Concentric Medical, Inc.
510(k) numberK131492
Submission
- Device name
- Modified Flowgate Balloon Guide Catheter
- Applicant
- Concentric Medical, Inc.
Mountain View, CA, US - Received
- May 23, 2013
- Decision date
- October 3, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DQY – Catheter, Percutaneous
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1250
- Specialty
- Cardiovascular
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Questions and answers
When was Modified Flowgate Balloon Guide Catheter cleared by the FDA?
Modified Flowgate Balloon Guide Catheter (K131492) received a 510(k) decision of Substantially Equivalent on October 3, 2013, 133 days after the submission was received.
What is the product code of K131492?
The FDA product code is DQY – Catheter, Percutaneous, a Class II (moderate risk) device regulated under 21 CFR 870.1250.