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

LEKSELL STEREOACTIC SYSTEM

K Number: K811726 · Decision Jul 10, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
60
Review Days
22

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Basic Information

Device Name
LEKSELL STEREOACTIC SYSTEM
K Number
K811726
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Downs Surgical , Ltd.
Date Received
June 18, 1981
Decision Date
July 10, 1981
Product Code
LHF
Advisory Committee
General Hospital
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LHF Warmer, Microwave, Infusion Fluid

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K Number Device Name
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K903750 ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-E
K903747 ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-U
K900611 SHEPPERD DILATATION TUBE SET (GS-501-20-H)
K900614 SHEPPERD SHORT MUSCLE RETRACTOR (GS-501-45-V)
K900612 SHEPPERD TREPHINE SET (GS-501-30-V)
K900610 SHEPPERD CANNULA STILLETTE & OBDURATOR SET
K900616 SHEPPERD CUTTING FORCEPS
K900609 SHEPPERD STRAIGHT AND CURVED NEEDLES
Search all 60 clearances from Downs Surgical , Ltd. →