Last synced on 14 November 2025 at 11:06 pm

QUICK-LYTE

Page Type
Cleared 510(K)
510(k) Number
K850209
510(k) Type
Traditional
Applicant
SERAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1985
Days to Decision
40 days

QUICK-LYTE

Page Type
Cleared 510(K)
510(k) Number
K850209
510(k) Type
Traditional
Applicant
SERAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1985
Days to Decision
40 days