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BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981747
510(k) Type
Traditional
Applicant
Sunscope Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1998
Days to Decision
94 days
Submission Type
Summary

BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981747
510(k) Type
Traditional
Applicant
Sunscope Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1998
Days to Decision
94 days
Submission Type
Summary