Last synced on 14 November 2025 at 11:06 pm

BRENTWOOD EZ SCAN 200 AMBULATORY ECG

Page Type
Cleared 510(K)
510(k) Number
K842976
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
214 days

BRENTWOOD EZ SCAN 200 AMBULATORY ECG

Page Type
Cleared 510(K)
510(k) Number
K842976
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
214 days