The following data is part of a premarket notification filed by Radionics, Inc. with the FDA for Contour Flex Valves (regular & Small).
| Device ID | K954285 |
| 510k Number | K954285 |
| Device Name: | CONTOUR FLEX VALVES (REGULAR & SMALL) |
| Classification | Shunt, Central Nervous System And Components |
| Applicant | RADIONICS, INC. 76 CAMBRIDGE ST. Burlington, MA 01803 |
| Contact | Linda Jalbert |
| Correspondent | Linda Jalbert RADIONICS, INC. 76 CAMBRIDGE ST. Burlington, MA 01803 |
| Product Code | JXG |
| CFR Regulation Number | 882.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-09-14 |
| Decision Date | 1996-01-26 |