Last synced on 14 November 2025 at 11:06 pm

NEUROFAX EEG 5532

Page Type
Cleared 510(K)
510(k) Number
K915096
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1992
Days to Decision
120 days
Submission Type
Statement

NEUROFAX EEG 5532

Page Type
Cleared 510(K)
510(k) Number
K915096
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1992
Days to Decision
120 days
Submission Type
Statement