Last synced on 14 November 2025 at 11:06 pm

MYOPULSE

Page Type
Cleared 510(K)
510(k) Number
K833928
510(k) Type
Traditional
Applicant
BIOMEDICAL DESIGN INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1984
Days to Decision
396 days

MYOPULSE

Page Type
Cleared 510(K)
510(k) Number
K833928
510(k) Type
Traditional
Applicant
BIOMEDICAL DESIGN INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1984
Days to Decision
396 days