Last synced on 16 May 2025 at 11:05 pm

MINIX/MINIX ST PULSE GENERATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932884
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
5/2/1994
Days to Decision
322 days
Submission Type
Summary

MINIX/MINIX ST PULSE GENERATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932884
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
5/2/1994
Days to Decision
322 days
Submission Type
Summary