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

ARTHROSCOPIC SURGICAL POWER DEVICE

K Number: K863696 · Decision Sep 29, 1986
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
366
Applicant Total
89
Review Days
7

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Basic Information

Device Name
ARTHROSCOPIC SURGICAL POWER DEVICE
K Number
K863696
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
American Edwards Laboratories
Date Received
September 22, 1986
Decision Date
September 29, 1986
Product Code
KIT
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
KIT Media And Components, Synthetic Cell And Tissue Culture

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Other Clearances by American Edwards Laboratories

K Number Device Name
K873485 EDSLAB (R) OCCLUSION BALLOON CATHETER
K872596 TRANTEC DISPOSABLE PRESSURE TRANS.53-600/F/F30
K872529 THERMODILUTION CARDIAC OUTPUT COMPUTER, MOD. COM-2
K870444 HOMEPRO II VOLUMETRIC INFUSION PUMP
K864997 MEDTRAC VP VOLUMETRIC INFUSION PUMP
K864330 SHEAR FORCE GAUGE
K862724 VEIN VALVE CUTTER
K864155 MODIFICATION OF CARPENTIER-EDWARDS BIOPROSTHESIS
K863596 CHIN-FOGARTY INFLATION DEVICE
K863986 XENON LIGHT SOURCE FOR ENDOSCOPIC PROCEDURES
Search all 89 clearances from American Edwards Laboratories →