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SENSOCOR(TM) DIASYS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881771
510(k) Type
Traditional
Applicant
SENSORMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1989
Days to Decision
261 days

SENSOCOR(TM) DIASYS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881771
510(k) Type
Traditional
Applicant
SENSORMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1989
Days to Decision
261 days