Last synced on 20 May 2022 at 11:05 pm

VOLUREX II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833337
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1983
Days to Decision
62 days

VOLUREX II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833337
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1983
Days to Decision
62 days