Atlas FDA

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7

FDA 510(k) clearance K854612 · decided 1986-01-03

Clearance details

K-number
K854612
Device name
ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7
Applicant
Med-West, Inc.
Decision
Unknown
Date received
1985-11-18
Decision date
1986-01-03
Days to decision
46 days
Clearance type
Traditional
Product code
LFK
Device class
2
Regulation number
876.5540
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH) (K971897)Medron, Inc.1997-10-21
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET (K914936)Akcess Medical Products, Inc.1992-04-23
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS (K915215)Akcess Medical Products, Inc.1992-03-27
FC-101 FEMORAL CATHETER GUIDE WIRE (K891764)Akcess Medical Products, Inc.1989-04-07
FC-100 FEMORAL CATHETER (K891763)Akcess Medical Products, Inc.1989-04-07
MODIFICATION HEMOFILTRATION CATHETER HF-100 (K890717)Vas-Cath, Inc.1989-04-05
CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY (K880775)Medsurg Industries, Inc.1988-07-25
VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER (K882466)Vas-Cath, Inc.1988-07-13
NEW SECOND FRENCH SIZE MAHURKAR CATHETER (K865096)Quinton, Inc.1987-02-18
CYTOSTATIC FILTRATION SET (K863218)Meadox Surgimed, Inc.1987-02-12
MEDCOMP C.A.V.H. CATHETER (K862771)Medical Components, Inc.1986-08-06
MEDCOMP'S FEMORAL VEIN CATHETERS (K860810)Medical Components, Inc.1986-04-08

Recalls involving this device

No recalls on record reference this clearance.