510(k) K943831
K943831 is an FDA 510(k) premarket notification submitted by Orion Life Systems, Inc. for the device "PRE-FILLED 30CC INFLATION SYRINGE W/STERILE WATER". The FDA issued a decision of Substantially Equivalent on November 21, 1994. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Orion Life Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 21, 1994
- Date Received
- August 5, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter And Tip, Suction
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type