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NIHON KOHDEN TEC-7511A/TEC-7521A CARDIOLIFE PORTABLE DEFIBRILLATOR AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971436
510(k) Type
Traditional
Applicant
Nihon Kohden America, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
10/21/1997
Days to Decision
186 days

NIHON KOHDEN TEC-7511A/TEC-7521A CARDIOLIFE PORTABLE DEFIBRILLATOR AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971436
510(k) Type
Traditional
Applicant
Nihon Kohden America, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
10/21/1997
Days to Decision
186 days