Last synced on 14 November 2025 at 11:06 pm

CARDIOVASCULAR DEVICES

Page Type
Cleared 510(K)
510(k) Number
K820045
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
22 days

CARDIOVASCULAR DEVICES

Page Type
Cleared 510(K)
510(k) Number
K820045
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
22 days