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VIVALITH 5, - MDL-201A & TDL-201A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801763
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1980
Days to Decision
30 days

VIVALITH 5, - MDL-201A & TDL-201A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801763
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1980
Days to Decision
30 days