510(k) K894072
K894072 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "THE PUDENZ IN LINE VALVE". The FDA issued a decision of Substantially Equivalent on Aug 7, 1989. The device falls under product code JXG (Shunt, Central Nervous System And Components), a Class II device regulated under 21 CFR 882.5550. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 7, 1989
- Date Received
- Jun 8, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Shunt, Central Nervous System And Components
- Device Class
- Class II
- Regulation Number
- 882.5550
- Review Panel
- NE
- Submission Type
- 510(k)