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PHILIPS HEARTSTART FR2+ AUTOMATED EXTERNAL DEFIBRILLATOR, MODELS M3860A, M3861A, M3840A, M3841A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051632
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2005
Days to Decision
107 days
Submission Type
Summary

PHILIPS HEARTSTART FR2+ AUTOMATED EXTERNAL DEFIBRILLATOR, MODELS M3860A, M3861A, M3840A, M3841A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051632
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2005
Days to Decision
107 days
Submission Type
Summary