510(k) K081718
K081718 is an FDA 510(k) premarket notification submitted by Atrium Medical Corp. for the device "EXPRESS CHEST DRAIN". The FDA issued a decision of Substantially Equivalent on July 25, 2008. The device falls under product code KDQ (Bottle, Collection, Vacuum), a Class II device regulated under 21 CFR 880.6740. Atrium Medical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 25, 2008
- Date Received
- June 18, 2008
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bottle, Collection, Vacuum
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type