Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
- MiscellaneousMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart C—General Hospital and Personal Use Monitoring DevicesCFR Sub-Part
- Subpart D—Pathology Instrumentation and AccessoriesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- LKGPort & Catheter, Implanted, Subcutaneous, Intraventricular2Product Code
- K950315CORDIS CSF RESERVOIR2Cleared 510(K)
- K881690PORT-A-CATH PORTAL INTRODUCER FORCEPS2Cleared 510(K)
- K881493PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF.2Cleared 510(K)
- K874468P-S MEDICAL VENTRICULAR ACCESS PORT2Cleared 510(K)
- K874498CSF-VENTRICULOSTOMY RESERVOIR2Cleared 510(K)
- K833822P-S MEDICAL CSF ACCESS DEV 15MM/25MM2Cleared 510(K)
- K833672HH SUBCUTANEOUS ACCESS PORT2Cleared 510(K)
- K823790VENTRICULAR ACCESS SYSTEM2Cleared 510(K)
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- HematologyReview Panel
- ImmunologyReview Panel
- MicrobiologyReview Panel
- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
CORDIS CSF RESERVOIR
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K950315
- 510(k) Type
- Traditional
- Applicant
- CORDIS CORP.
- Country
- United States
- FDA Decision
- Substantially Equivalent - Kit
- Decision Date
- 5/9/1995
- Days to Decision
- 103 days
- Submission Type
- Summary