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TEC-8251A DEFIBRILLATOR MONITOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914971
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1991
Days to Decision
47 days
Submission Type
Statement

TEC-8251A DEFIBRILLATOR MONITOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914971
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1991
Days to Decision
47 days
Submission Type
Statement