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KONTRON KOLORMON PLUS ECG WITH RESPIRATION MODULE

Page Type
Cleared 510(K)
510(k) Number
K971038
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/24/1997
Days to Decision
188 days
Submission Type
Statement

KONTRON KOLORMON PLUS ECG WITH RESPIRATION MODULE

Page Type
Cleared 510(K)
510(k) Number
K971038
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/24/1997
Days to Decision
188 days
Submission Type
Statement