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FI02 SENSING MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944120
510(k) Type
Traditional
Applicant
CORE-M, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1995
Days to Decision
260 days
Submission Type
Statement

FI02 SENSING MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944120
510(k) Type
Traditional
Applicant
CORE-M, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1995
Days to Decision
260 days
Submission Type
Statement