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MODIFIED SEISMOCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K900130
510(k) Type
Traditional
Applicant
SEISMED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1990
Days to Decision
82 days

MODIFIED SEISMOCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K900130
510(k) Type
Traditional
Applicant
SEISMED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1990
Days to Decision
82 days