Last synced on 14 November 2025 at 11:06 pm

BAXTER NIGHT EXCH DEVICE(NXD) PERITONEAL DIALY SYST

Page Type
Cleared 510(K)
510(k) Number
K935659
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
225 days
Submission Type
Summary

BAXTER NIGHT EXCH DEVICE(NXD) PERITONEAL DIALY SYST

Page Type
Cleared 510(K)
510(k) Number
K935659
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
225 days
Submission Type
Summary