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

VALVED TEARAWAY INTRODUCER GENERATION II

K Number: K124046 · Decision Jun 3, 2013
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
63
Review Days
154

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
VALVED TEARAWAY INTRODUCER GENERATION II
K Number
K124046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medical Components, Inc.
Date Received
December 31, 2012
Decision Date
June 3, 2013
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DYB Introducer, Catheter

Similar 510(k) Clearances

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

View all

Other Clearances by Medical Components, Inc.

K Number Device Name
K250836 14F Duo-Flow® Side X Side Double Lumen Catheter
K141633 PRO-PICC WITH VALVE TECHNOLOGY
K132880 MEDCOMP POWER INJECTABLE SAFETY HUBER NEEDLE
K131687 6F X 60CM TRIPLE PRO-LINE CT BASIC IR SET
K130687 2F & 3F VASCU-SHEATH TEARAWAY INTRODUCER
K130923 5F DIGNITY CT TITANIUM PORT
K123617 3F PRO-PICC
K122423 VASU-PICC
K121848 SPLIT CATH III 24CM SPLIT CATH III 24CM SPLIT CATH III 32CM CATH III 36CM SPLIT CATH III 40CM AND 55CM
K120281 DIGNITY POWER INJECTABLE TITANIUM PORT
Search all 63 clearances from Medical Components, Inc. →