510(k) K950677
K950677 is an FDA 510(k) premarket notification submitted by Atrium Medical Corp. for the device "ATRIUM DRY SUCTION CONTROL WATER SEAL CHEST DRAIN". The FDA issued a decision of Substantially Equivalent on April 13, 1995. 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
- April 13, 1995
- Date Received
- February 14, 1995
- Clearance Type
- Traditional
- 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