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HEARTSTART 2000, MANUAL DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871136
510(k) Type
Traditional
Applicant
FIRST MEDICAL DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1987
Days to Decision
53 days

HEARTSTART 2000, MANUAL DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871136
510(k) Type
Traditional
Applicant
FIRST MEDICAL DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1987
Days to Decision
53 days