Last synced on 23 September 2022 at 11:05 pm

EPIDURAL SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832778
510(k) Type
Traditional
Applicant
CONCORD LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1983
Days to Decision
41 days

EPIDURAL SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832778
510(k) Type
Traditional
Applicant
CONCORD LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1983
Days to Decision
41 days