FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LEKSELL STEREOTACTIC SYSTEM

K Number: K802140 · Decision Feb 5, 1981
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
9
Applicant Total
60
Review Days
154

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Basic Information

Device Name
LEKSELL STEREOTACTIC SYSTEM
K Number
K802140
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1920
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Downs Surgical , Ltd.
Date Received
September 4, 1980
Decision Date
February 5, 1981
Product Code
IWY
Advisory Committee
Radiology
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
IWY Holder, Head, Radiographic

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Other Clearances by Downs Surgical , Ltd.

K Number Device Name
K903749 ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-U
K903748 ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-V
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
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