510(k) K173803
K173803 is an FDA 510(k) premarket notification submitted by B.Braun Medical, Inc. for the device "Omnican fine". The FDA issued a decision of Substantially Equivalent on Jun 11, 2018. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. B.Braun Medical, Inc. has 149 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 11, 2018
- Date Received
- Dec 15, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Hypodermic, Single Lumen
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type
- 510(k)