Last synced on 16 May 2025 at 11:05 pm

MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910237
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1991
Days to Decision
38 days

MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910237
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1991
Days to Decision
38 days