Last synced on 14 November 2025 at 11:06 pm

COLLATEK POWDER

Page Type
Cleared 510(K)
510(k) Number
K012990
510(k) Type
Traditional
Applicant
BIOCORE MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
48 days
Submission Type
Summary

COLLATEK POWDER

Page Type
Cleared 510(K)
510(k) Number
K012990
510(k) Type
Traditional
Applicant
BIOCORE MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
48 days
Submission Type
Summary