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

PERITONEAL DIALYSIS CYCLER SET (8UNIT)

K Number: K812772 · Decision Oct 19, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
16
Review Days
14

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PERITONEAL DIALYSIS CYCLER SET (8UNIT)
K Number
K812772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Dravon Medical, Inc.
Date Received
October 5, 1981
Decision Date
October 19, 1981
Product Code
KDJ
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
KDJ Set, Administration, For Peritoneal Dialysis, Disposable

Similar 510(k) Clearances

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

View all

Other Clearances by Dravon Medical, Inc.

K Number Device Name
K873455 S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS
K860770 AM-100 I/A AMPAC
K832739 STEDIFLO INFUSION SET
K831842 DRAVON T CLAMP
K812771 PERITONEAL DIALYSIS DRAINAGE
K811851 S-610 SHUNT ADAPTOR SET
K800435 HEMOSTATIC/TUBE OCCLUDING FORCEPS
K782057 CATHETER, RADIOPAQUE TENCKHOFF
K782058 CATHETER, BETA-CAP-PERITONEAL
K781755 DAP-PAK
Search all 16 clearances from Dravon Medical, Inc. →