Last synced on 31 March 2023 at 11:04 pm

CDX 200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820035
510(k) Type
Traditional
Applicant
CDX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1982
Days to Decision
62 days

CDX 200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820035
510(k) Type
Traditional
Applicant
CDX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1982
Days to Decision
62 days