Last synced on 14 November 2025 at 11:06 pm

PERITONEAL CATHETER-CHANGES-

Page Type
Cleared 510(K)
510(k) Number
K833749
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1983
Days to Decision
62 days

PERITONEAL CATHETER-CHANGES-

Page Type
Cleared 510(K)
510(k) Number
K833749
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1983
Days to Decision
62 days