Last synced on 20 May 2022 at 11:05 pm

O2 CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780750
510(k) Type
Traditional
Applicant
DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1978
Days to Decision
80 days

O2 CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780750
510(k) Type
Traditional
Applicant
DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1978
Days to Decision
80 days