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

DISPOSABLE CONSTRAST DELIVERY SPIKE KIT

K Number: K802329 · Decision Oct 3, 1980
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
19
Review Days
10

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Basic Information

Device Name
DISPOSABLE CONSTRAST DELIVERY SPIKE KIT
K Number
K802329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Stanco Medical, Inc.
Date Received
September 23, 1980
Decision Date
October 3, 1980
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

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Other Clearances by Stanco Medical, Inc.

K Number Device Name
K810642 ATRIAL-VENTRICULAR PACING ELECTRODE KIT
K810643 UNIVERSAL PACING ELECTRODE KIT
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. →