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

4-SURE NELATON CATHETER

K Number: K931048 · Decision Feb 14, 1994
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
81
Applicant Total
11
Review Days
350

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Basic Information

Device Name
4-SURE NELATON CATHETER
K Number
K931048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Boston Pacific Medical, Inc.
Date Received
March 1, 1993
Decision Date
February 14, 1994
Product Code
EZD
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
EZD Catheter, Straight

Similar 510(k) Clearances

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Other Clearances by Boston Pacific Medical, Inc.

K Number Device Name
K933109 4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS
K922402 4 SURE TM ENTERAL FEEDING BAG
K931047 4-SURE FEMALE CATHETER
K921852 4 SURE TM RECTAL TUBE
K921853 4 SURE TM FEEDING TUBES
K921851 4 SURE TM SUCTION CATHETERS & KITS
K922398 4 SURE TM ENEMA BAG SET
K922397 4 SURE TM NASAL OXYGEN CANNULA
K924995 4 SURE TM ANESTHESIA EXTENSION SET
K922401 4 SURE TM COLOSTOMY POUCH
Search all 11 clearances from Boston Pacific Medical, Inc. →