510(k) K790221
- Device
- Pulse Generator, Cyberlith Implantable
- Applicant
- INTERMEDICS, INC.
- 510(k) number
- K790221
- Decision
- Unknown (SESP)
- Decision date
- 1979-01-30
- Date received
- 1979-01-30
- Review panel
- Unknown
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents#
510(k) summary PDF not indicated by FDA