LKG — Port & Catheter, Implanted, Subcutaneous, Intraventricular Class II
FDA Device Classification
Classification Details
- Product Code
- LKG
- Device Class
- Class II
- Regulation Number
- 882.5550
- Submission Type
- Review Panel
- HO
- Medical Specialty
- Neurology
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K950315 | cordis | CORDIS CSF RESERVOIR | May 9, 1995 |
| K881690 | pharmacia deltec | PORT-A-CATH PORTAL INTRODUCER FORCEPS | May 20, 1988 |
| K881493 | pharmacia deltec | PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF. | May 20, 1988 |
| K874468 | pudenz-schulte medical research | P-S MEDICAL VENTRICULAR ACCESS PORT | February 11, 1988 |
| K874498 | pudenz-schulte medical research | CSF-VENTRICULOSTOMY RESERVOIR | February 11, 1988 |
| K833822 | pudenz-schulte medical research | P-S MEDICAL CSF ACCESS DEV 15MM/25MM | May 25, 1984 |
| K833672 | holter-hausner intl | HH SUBCUTANEOUS ACCESS PORT | March 6, 1984 |
| K823790 | american heyer schulte | VENTRICULAR ACCESS SYSTEM | April 28, 1983 |