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FEVER MONITORING KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931747
510(k) Type
Traditional
Applicant
POLYMEDICA HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/13/1993
Days to Decision
249 days
Submission Type
Statement

FEVER MONITORING KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931747
510(k) Type
Traditional
Applicant
POLYMEDICA HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
12/13/1993
Days to Decision
249 days
Submission Type
Statement