Last synced on 30 May 2025 at 11:05 pm

LIQUID FIBRINOGEN FDP CONTROL LEVEL 1 & 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934741
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1994
Days to Decision
342 days
Submission Type
Statement

LIQUID FIBRINOGEN FDP CONTROL LEVEL 1 & 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934741
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1994
Days to Decision
342 days
Submission Type
Statement