Last synced on 19 July 2024 at 11:05 pm

PERCUSSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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