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ABBOTT ALCYON(TM) 300 (WITHOUT ISE MODULE) AND 300I (WITH ISE MODULE) ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K974779
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1998
Days to Decision
53 days
Submission Type
Summary

ABBOTT ALCYON(TM) 300 (WITHOUT ISE MODULE) AND 300I (WITH ISE MODULE) ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K974779
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1998
Days to Decision
53 days
Submission Type
Summary