Last synced on 2 December 2022 at 11:04 pm

PERITONEAL CYCLER & MANIFOLD SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772136
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1977
Days to Decision
36 days

PERITONEAL CYCLER & MANIFOLD SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772136
510(k) Type
Traditional
Applicant
PHYSIO-CONTROL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1977
Days to Decision
36 days