FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IMPRA PERITONEAL CATHETER

K Number: K823857 · Decision Jan 26, 1983
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
81
Applicant Total
29
Review Days
35

Basic Information

Device Name
IMPRA PERITONEAL CATHETER
K Number
K823857
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
IMPRA, INC.
Date Received
December 22, 1982
Decision Date
January 26, 1983
Product Code
FKX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FKX System, Peritoneal, Automatic Delivery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FKX), ordered by most recent decision date.

View all

Other Clearances by IMPRA, INC.

K Number Device Name
K004012 IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
K004011 IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS
K991027 BI-DIRECTIONAL TUNNELER
K983769 DISTAFLO BYPASS GRAFT
K983861 DISTAFLO BYPASS GRAFT
K983064 IMPRA HIGH POROSITY GRAFT
K981079 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K981076 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K971192 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964877 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
Search all 29 clearances from IMPRA, INC. →