Last synced on 14 November 2025 at 11:06 pm

PCX-100 PATIENT INPUT LEADWIRE

Page Type
Cleared 510(K)
510(k) Number
K851632
510(k) Type
Traditional
Applicant
EATON MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1985
Days to Decision
204 days

PCX-100 PATIENT INPUT LEADWIRE

Page Type
Cleared 510(K)
510(k) Number
K851632
510(k) Type
Traditional
Applicant
EATON MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1985
Days to Decision
204 days