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

PERCUTANEOUS SHEATH INTRO. KIT OR TRAY

K Number: K792172 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
19
Review Days
15

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Basic Information

Device Name
PERCUTANEOUS SHEATH INTRO. KIT OR TRAY
K Number
K792172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Stanco Medical, Inc.
Date Received
October 29, 1979
Decision Date
November 13, 1979
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

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Other Clearances by Stanco Medical, Inc.

K Number Device Name
K810642 ATRIAL-VENTRICULAR PACING ELECTRODE KIT
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K802289 PERICARDIOCENTESIS KIT
K802288 SWAN GANZ CATHETER PLACEMENT KIT
K802287 RIGHT ATRIAL LINE KIT
K802259 TRANSVENOUS PACEMAKER ELECTRODE KIT
K802290 REGIONAL INTRAVENOUS ANESTHESIA KIT
K802326 PRESSURE MONITORING LINES
K802260 VASCULAR CATHETER WIREGUIDES
K802328 DISP. TOUGY-BORST TYPE ADAPTOR W/PORT
Search all 19 clearances from Stanco Medical, Inc. →