510(k) K832906
- Device
- Port-a-cath Implantable Catheter Sys
- Applicant
- PHARMACIA, INC.
- 510(k) number
- K832906
- Product code
- LLD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-03-06
- Date received
- 1983-08-29
- Regulation
- 880.5965
- Classification name
- Port & Catheter, Implanted, Subcutaneous, Intraperitoneal
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9617604
- 2032112
- 3012307300
Source Documents#
510(k) summary PDF not indicated by FDA