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ULTROSER G

Page Type
Cleared 510(K)
510(k) Number
K844413
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1985
Days to Decision
105 days

ULTROSER G

Page Type
Cleared 510(K)
510(k) Number
K844413
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1985
Days to Decision
105 days