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

Y-ADAPTER W/THOUY BORST

K Number: K895580 · Decision Apr 30, 1990
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
7
Review Days
227

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
Y-ADAPTER W/THOUY BORST
K Number
K895580
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Angeion Corp.
Date Received
September 15, 1989
Decision Date
April 30, 1990
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 Angeion Corp.

K Number Device Name
K921757 ANGEION IGITAL ANGEFLATOR
K925533 ANGESTAT(R) PERICARDIAL DRAINAGE SHEATH SET
K915719 ANGEION ENDOSCOPIC VALVE SEAL
K902377 ANGEFLATOR(TM)
K894446 ANGEION HEMOSTASIS VALVE INTRODUCER
K871153 CATHETER INTRODUCER