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ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990106
510(k) Type
Traditional
Applicant
BIO-DETEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
45 days
Submission Type
Statement

ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990106
510(k) Type
Traditional
Applicant
BIO-DETEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
45 days
Submission Type
Statement