Last synced on 9 May 2025 at 11:05 pm

CARPENTIER-EDWARDS FLEX. ANNULOPLASTY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792441
510(k) Type
Traditional
Applicant
EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking & Post-Market Surveillance
Decision Date
3/17/1980
Days to Decision
109 days

CARPENTIER-EDWARDS FLEX. ANNULOPLASTY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792441
510(k) Type
Traditional
Applicant
EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking & Post-Market Surveillance
Decision Date
3/17/1980
Days to Decision
109 days