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MODIFIED SEISMOCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K910994
510(k) Type
Traditional
Applicant
SEISMED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1992
Days to Decision
318 days

MODIFIED SEISMOCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K910994
510(k) Type
Traditional
Applicant
SEISMED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1992
Days to Decision
318 days