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DIATHERMY DEVICE-MICROFOCUS

Page Type
Cleared 510(K)
510(k) Number
K941567
510(k) Type
Traditional
Applicant
CHEUNG LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1996
Days to Decision
752 days
Submission Type
Statement

DIATHERMY DEVICE-MICROFOCUS

Page Type
Cleared 510(K)
510(k) Number
K941567
510(k) Type
Traditional
Applicant
CHEUNG LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1996
Days to Decision
752 days
Submission Type
Statement