Last synced on 14 November 2025 at 11:06 pm

ECG PATIENT MONITOR 302

Page Type
Cleared 510(K)
510(k) Number
K850155
510(k) Type
Traditional
Applicant
RIGEL MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
45 days

ECG PATIENT MONITOR 302

Page Type
Cleared 510(K)
510(k) Number
K850155
510(k) Type
Traditional
Applicant
RIGEL MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1985
Days to Decision
45 days