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

DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER

K Number: K042709 · Decision Jan 18, 2005
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
14
Review Days
110

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Basic Information

Device Name
DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER
K Number
K042709
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tyco Healthcare
Date Received
September 30, 2004
Decision Date
January 18, 2005
Product Code
EZL
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
EZL Catheter, Retention Type, Balloon

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Other Clearances by Tyco Healthcare

K Number Device Name
K071049 DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOR
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K070653 KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662
K061492 MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE
K040897 DOVER ROB-NEL CATHETER
K040649 KENDALL SCD EXPRESS KAMBIA THIGH LENGTH TEARAWAY SLEEVE
K041243 DOVER RED RUBBER ROBINSON CATHETER
K032438 MODIFICATION TO: MONOJET PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE, MONOJET PREFILL HEPRIN LOCK FLUSH SYRINGE
K033453 KENDALL ULTEC PRO AG+ HYDROCOLLOID DRESSING
K032827 KENDALL LIFETRACE UMBILICAL BLOOD COLLECTION KIT, CODE 56501
Search all 14 clearances from Tyco Healthcare →