FDA Product Code
FDA Product Code LKG — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.5550
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K950315 | CORDIS CSF RESERVOIR | Cordis Corp. | 1995-05-09 | Traditional | PDF ↗ |
| K881690 | PORT-A-CATH PORTAL INTRODUCER FORCEPS | Pharmacia Deltec, Inc. | 1988-05-20 | Traditional | PDF ↗ |
| K881493 | PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF. | Pharmacia Deltec, Inc. | 1988-05-20 | Traditional | PDF ↗ |
| K874498 | CSF-VENTRICULOSTOMY RESERVOIR | Pudenz-Schulte Medical Research Corp. | 1988-02-11 | Traditional | PDF ↗ |
| K874468 | P-S MEDICAL VENTRICULAR ACCESS PORT | Pudenz-Schulte Medical Research Corp. | 1988-02-11 | Traditional | PDF ↗ |
| K833822 | P-S MEDICAL CSF ACCESS DEV 15MM/25MM | Pudenz-Schulte Medical Research Corp. | 1984-05-25 | Traditional | PDF ↗ |
| K833672 | HH SUBCUTANEOUS ACCESS PORT | Holter-Hausner Intl. | 1984-03-06 | Traditional | PDF ↗ |
| K823790 | VENTRICULAR ACCESS SYSTEM | American Heyer Schulte | 1983-04-28 | Traditional | PDF ↗ |
Product code LKG · Class II · Neurology. Data: openFDA.