FDA Product Code
FDA Product Code GWM — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.1620
510(k) Clearances — 105 records · page 2 of 2
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K802138 | CHEEK TOOL SET | Codman & Shurtleff, Inc. | 1980-10-31 | Traditional | PDF ↗ |
| K802100 | INTRACRANIAL PRESSURING MONITORING SYST. | Pudenz-Schulte Medical Research Corp. | 1980-09-16 | Traditional | PDF ↗ |
| K801755 | MMI/GAELTEC CATHETER TIP PRESSURE | Medical Measurements, Inc. | 1980-08-13 | Traditional | PDF ↗ |
| K790920 | INTRACRANIAL PRESSURE MONITORING | Codman & Shurtleff, Inc. | 1979-08-03 | Traditional | PDF ↗ |
| K772063 | CATHETER, INTRACRANIAL PRESS. MONITOR. | Cordis Corp. | 1978-01-03 | Traditional | PDF ↗ |
Product code GWM · Class II · Neurology. Data: openFDA.