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MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032721
510(k) Type
Special
Applicant
STELLARTECH RESEARCH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
33 days
Submission Type
Summary

MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032721
510(k) Type
Special
Applicant
STELLARTECH RESEARCH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2003
Days to Decision
33 days
Submission Type
Summary