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PERCUSSOR

Page Type
Cleared 510(K)
510(k) Number
K812166
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1981
Days to Decision
19 days

PERCUSSOR

Page Type
Cleared 510(K)
510(k) Number
K812166
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1981
Days to Decision
19 days