FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

MEGA LUMBAR PUNCTURE KIT

K Number: K910089 · Decision Jun 20, 1991
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
5
Applicant Total
50
Review Days
162

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Basic Information

Device Name
MEGA LUMBAR PUNCTURE KIT
K Number
K910089
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2500
Medical Specialty
General Hospital
Decision
Unknown
Applicant
Megadyne Medical Products, Inc.
Date Received
January 9, 1991
Decision Date
June 20, 1991
Product Code
FMJ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FMJ Manometer, Spinal-Fluid

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K213696 ETHICON Megadyne Electrosurgical Generator
K200250 Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor
K193145 Ethicon Megadyne Electrosurgical Generator, Bipolar Footswitch
K191328 Megadyne Foot Switch
K141587 E-Z CLEAR SMOKE EVACUATION ELECTROSURGICAL PENCIL;CLEAR NOZZLE EXTENTION, ULPA FILTER, CHARCOAL FILTER, ADAPTER
K133726 MEGA SOFT UNIVERSAL PATIENT RETURN ELECTRODE
K080741 MEGA SOFT REUSABLE PATIENT RETURN ELECTRODE
K081791 E-Z CLEAN ELECTROSURGICAL ELECTRODE
K072559 SUCTION COAGULATOR
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