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SENTINEL AMMONIA ULTRA DIAGNOSTIC ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051114
510(k) Type
Traditional
Applicant
SENTINEL CH. SRL
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/25/2005
Days to Decision
207 days
Submission Type
Summary

SENTINEL AMMONIA ULTRA DIAGNOSTIC ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051114
510(k) Type
Traditional
Applicant
SENTINEL CH. SRL
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/25/2005
Days to Decision
207 days
Submission Type
Summary