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MYOPACH ULTRASONIC PACHOMETER

Page Type
Cleared 510(K)
510(k) Number
K844112
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1986
Days to Decision
450 days

MYOPACH ULTRASONIC PACHOMETER

Page Type
Cleared 510(K)
510(k) Number
K844112
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1986
Days to Decision
450 days