Last synced on 30 May 2025 at 11:05 pm

CARDIOPAC DEFIBRILLATOR 444

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844103
510(k) Type
Traditional
Applicant
BIRTCHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1985
Days to Decision
87 days

CARDIOPAC DEFIBRILLATOR 444

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844103
510(k) Type
Traditional
Applicant
BIRTCHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1985
Days to Decision
87 days