FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS

K Number: K933109 · Decision Mar 28, 1994
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
11
Review Days
276

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
4SURE URO-LINK UROLOGICAL PROCEDURE TRAYS
K Number
K933109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Statement
Applicant
Boston Pacific Medical, Inc.
Date Received
June 25, 1993
Decision Date
March 28, 1994
Product Code
KOD
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
KOD Catheter, Urological

Similar 510(k) Clearances

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

View all

Other Clearances by Boston Pacific Medical, Inc.

K Number Device Name
K922402 4 SURE TM ENTERAL FEEDING BAG
K931048 4-SURE NELATON CATHETER
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. →