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

ATRIAL-VENTRICULAR PACING ELECTRODE KIT

K Number: K810642 · Decision Apr 8, 1981
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
127
Applicant Total
19
Review Days
29

Basic Information

Device Name
ATRIAL-VENTRICULAR PACING ELECTRODE KIT
K Number
K810642
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
STANCO MEDICAL, INC.
Date Received
March 10, 1981
Decision Date
April 8, 1981
Product Code
LDF
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
LDF Electrode, Pacemaker, Temporary

Similar 510(k) Clearances

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

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Other Clearances by STANCO MEDICAL, INC.

K Number Device Name
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
K802260 VASCULAR CATHETER WIREGUIDES
K802326 PRESSURE MONITORING LINES
K802327 SHEATH DILATOR SET
K802328 DISP. TOUGY-BORST TYPE ADAPTOR W/PORT
Search all 19 clearances from STANCO MEDICAL, INC. →