Last synced on 14 November 2025 at 11:06 pm

ELECTROSTIMULATOR MODEL 808

Page Type
Cleared 510(K)
510(k) Number
K880426
510(k) Type
Traditional
Applicant
CORNELL ENTERPRISES CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1988
Days to Decision
231 days

ELECTROSTIMULATOR MODEL 808

Page Type
Cleared 510(K)
510(k) Number
K880426
510(k) Type
Traditional
Applicant
CORNELL ENTERPRISES CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1988
Days to Decision
231 days