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REVEAL INSERTABLE LOOP RECORDER (ILR) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972242
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
1/16/1998
Days to Decision
214 days

REVEAL INSERTABLE LOOP RECORDER (ILR) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972242
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
1/16/1998
Days to Decision
214 days