Last synced on 14 November 2025 at 11:06 pm

ACCESS CARDIOSYSTEMS MANUAL DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K011461
510(k) Type
Traditional
Applicant
ACCESS CARDIOSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2002
Days to Decision
379 days
Submission Type
Summary

ACCESS CARDIOSYSTEMS MANUAL DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K011461
510(k) Type
Traditional
Applicant
ACCESS CARDIOSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2002
Days to Decision
379 days
Submission Type
Summary