Last synced on 25 April 2025 at 11:05 pm

PROTIME MICROCOAGULATION SYSTEM / PROTIME 3 CUVETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010599
510(k) Type
Special
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2001
Days to Decision
124 days
Submission Type
Summary

PROTIME MICROCOAGULATION SYSTEM / PROTIME 3 CUVETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010599
510(k) Type
Special
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2001
Days to Decision
124 days
Submission Type
Summary