Last synced on 14 November 2025 at 11:06 pm

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990325
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1999
Days to Decision
142 days
Submission Type
Summary

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990325
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1999
Days to Decision
142 days
Submission Type
Summary