Last synced on 16 May 2025 at 11:05 pm

PULSE GENERATOR, R WAVE DEMAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790141
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1979
Days to Decision
203 days

PULSE GENERATOR, R WAVE DEMAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790141
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1979
Days to Decision
203 days