510(k) K771986
- Device
- Catheter, Mediastinal&pericardial
- Applicant
- THE MINNESOTA BACK BRACE CO.
- 510(k) number
- K771986
- Product code
- FHF
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-10-28
- Date received
- 1977-10-19
- Regulation
- 876.4370
- Classification name
- System, Evacuator, Fluid
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- 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#
- 2531475
- 3007421149
- 3009051888
- 1820334
- 2027062
- 2916714
- 3032953156
- 3009763019
- 9680721
- 2027111
- 3016096097
- 8040510
Source Documents#
510(k) summary PDF not indicated by FDA