Advance 18LP Pta Dilatation Catheter
FDA 510(k) K073378 · Cook, Inc.
510(k) numberK073378
Submission
- Device name
- Advance 18LP Pta Dilatation Catheter
- Applicant
- Cook, Inc.
Bloomington, IN, US - Received
- December 3, 2007
- Decision date
- December 28, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 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 Advance 18LP Pta Dilatation Catheter cleared by the FDA?
Advance 18LP Pta Dilatation Catheter (K073378) received a 510(k) decision of Substantially Equivalent on December 28, 2007, 25 days after the submission was received.
What is the product code of K073378?
The FDA product code is DQY – Catheter, Percutaneous, a Class II (moderate risk) device regulated under 21 CFR 870.1250.