Atlas FDA

CATHETER, PERITONEAL DIALYSIS

FDA 510(k) clearance K760544 · decided 1976-10-20

Clearance details

K-number
K760544
Device name
CATHETER, PERITONEAL DIALYSIS
Applicant
Travenol Laboratories, S.A.
Decision
Substantially Equivalent
Date received
1976-08-30
Decision date
1976-10-20
Days to decision
51 days
Clearance type
Traditional
Product code
FKO
Device class
2
Regulation number
876.5630
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, 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
CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS (K964514)Corpak, Inc.1998-06-26
PERITONEAL DIALYSIS CATHETER CONNECTOR (K974570)Medigroup, Inc.1998-02-27
TITANIUM CONNECTOR (2 PART) (K910787)Accurate Surgical Instruments Co.1991-08-15
AMUKIN 50% - AIRSPRAY(R) (K885037)Bernard J. Cooney, P.A.1990-10-19
PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM) (K874650)Quinton, Inc.1987-12-09
DIALY-NATE SET & DIALY-NATE CATHETER (K872221)Gesco Intl., Inc.1987-10-13
MODIFIED USE OF PULL-APART INTRODUCER SET (K871730)Quinton, Inc.1987-05-18
ACUTE PERITONEAL DIALYSIS KIT (K870472)Quinton, Inc.1987-02-25
PERITONEAL LAVAGE CATH PLC-8,SET PLS-8, KIT PLK-8 (K860155)Medical Components, Inc.1986-02-14
ACUTE PERITONEAL DIALYSIS CATHETERS (K854966)Thermedics, Inc.1986-01-09
CAPD STAGED CONNECTOR (K845041)Abbott Laboratories1985-02-21
LAZARUS-NELSON PERITONEAL LAVAGE TRAY (K813336)American Pharmaseal Div. Ahsc1981-12-18

Recalls involving this device

No recalls on record reference this clearance.