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PREAMPLIFIER MODULE, EKG RESPIRATION

Page Type
Cleared 510(K)
510(k) Number
K790304
510(k) Type
Traditional
Applicant
ABBOTT MEDICAL ELECTRONICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1979
Days to Decision
14 days

PREAMPLIFIER MODULE, EKG RESPIRATION

Page Type
Cleared 510(K)
510(k) Number
K790304
510(k) Type
Traditional
Applicant
ABBOTT MEDICAL ELECTRONICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1979
Days to Decision
14 days