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TECHNICON H* 3 RTX SYSTEM (IN-VITRO DIAG. SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K930148
510(k) Type
Traditional
Applicant
HERAEUS KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
119 days
Submission Type
Summary

TECHNICON H* 3 RTX SYSTEM (IN-VITRO DIAG. SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K930148
510(k) Type
Traditional
Applicant
HERAEUS KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
119 days
Submission Type
Summary