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

GLASSMAN SILICONE CATHETER

K Number: K934895 · Decision Oct 13, 1994
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
28
Review Days
373

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
GLASSMAN SILICONE CATHETER
K Number
K934895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Axiom Medical, Inc.
Date Received
October 5, 1993
Decision Date
October 13, 1994
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

Similar 510(k) Clearances

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

View all

Other Clearances by Axiom Medical, Inc.

K Number Device Name
K993592 AXIOM MULTIPURPOSE WOUND DRAIN
K971851 INTERPLEURAL ANESTHESIA CATHETER
K965146 FLAT CLOSED WOUND DRAIN WITH TROCAR
K922760 ATRAUM WOUND DRESSING--MODIFICATION
K905422 PVC ROUND WOUND DRAINS
K904218 SUCTION SYSTEM
K904133 DISPOSABLE FLUID COLLECTION BAG
K863247 AXIOM TROCAR THORACIC CATHETER
K861306 SUCTION SYSTEM
K852614 ATRAUM WOUND DRESSING
Search all 28 clearances from Axiom Medical, Inc. →