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AUTOREADER CALIBRATION TEST PLATE

Page Type
Cleared 510(K)
510(k) Number
K900579
510(k) Type
Traditional
Applicant
BIO-TEK INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1990
Days to Decision
20 days

AUTOREADER CALIBRATION TEST PLATE

Page Type
Cleared 510(K)
510(k) Number
K900579
510(k) Type
Traditional
Applicant
BIO-TEK INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1990
Days to Decision
20 days