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OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971840
510(k) Type
Traditional
Applicant
Invivo Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1998
Days to Decision
289 days
Submission Type
Statement

OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971840
510(k) Type
Traditional
Applicant
Invivo Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1998
Days to Decision
289 days
Submission Type
Statement