Last synced on 16 May 2025 at 11:05 pm

PULSE GENERATOR MODEL 629

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790670
510(k) Type
Traditional
Applicant
ELEMA-SCHONANDER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1979
Days to Decision
82 days

PULSE GENERATOR MODEL 629

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790670
510(k) Type
Traditional
Applicant
ELEMA-SCHONANDER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1979
Days to Decision
82 days