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

SIXALYZER

K Number: K880230 · Decision Mar 16, 1988
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
60
Applicant Total
11
Review Days
56

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Basic Information

Device Name
SIXALYZER
K Number
K880230
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1925
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Lukens Corp.
Date Received
January 20, 1988
Decision Date
March 16, 1988
Product Code
IKK
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IKK System, Isokinetic Testing And Evaluation

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Other Clearances by Lukens Corp.

K Number Device Name
K800102 STANFORD STERILE LAP SPONGES
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K791495 LUKENS BONE WAX (GAMMA RADIATION)
K770797 TRAY, CATHETERIZATION W/FOLEY, STERILE
K770795 SHAVE PREP SET
K770799 TRAY, IRRIGATION, STERILE, BASIC
K770796 SKIN SCRUB PREP SET
K770794 SUTURE REMOVAL SET, STERILE
K770798 BLADES, SURGICAL, STERILE
K770800 HANDLES, BLADE, SURGICAL
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