Atlas FDA

PD CATH

FDA 510(k) clearance K053123 · decided 2006-03-29

Clearance details

K-number
K053123
Device name
PD CATH
Applicant
Med-Conduit, Inc.
Decision
Substantially Equivalent
Date received
2005-11-07
Decision date
2006-03-29
Days to decision
142 days
Clearance type
Traditional
Product code
FJS
Device class
2
Regulation number
876.5630
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Tyngsboro, MA, US
Third-party review
No
Expedited review
No

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FALLER TROCAR (K120130)Medigroup, Inc.2012-05-21
VETA PERITONEAL DIALYSIS CATHETER (K113354)Pfm Medical, Inc.2012-03-13
FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560 (K071167)Medigroup, Inc.2007-08-31
FLEX-NECK ARC CATHETER (K070730)Medigroup, Inc.2007-07-03
EMBEDDING TOOL, MODEL TE-1000 (K060897)Medigroup, Inc.2006-07-18
FLEX-NECK PD CATHETER, INFANT (K031351)Medigroup, Inc.2003-09-17
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Recalls involving this device

No recalls on record reference this clearance.