510(k) K152625
K152625 is an FDA 510(k) premarket notification submitted by Micro Medical Solutions, Inc. for the device "MMS Guide Catheter". The FDA issued a decision of Substantially Equivalent on Mar 9, 2016. The device falls under product code KRA (Catheter, Continuous Flush), a Class II device regulated under 21 CFR 870.1210. Micro Medical Solutions, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 9, 2016
- Date Received
- Sep 15, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Continuous Flush
- Device Class
- Class II
- Regulation Number
- 870.1210
- Review Panel
- CV
- Submission Type
- 510(k)