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

FIRM-A-TRON MARK X

K Number: K843583 · Decision Nov 29, 1984
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
5
Review Days
79

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Basic Information

Device Name
FIRM-A-TRON MARK X
K Number
K843583
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Biotron , Ltd.
Date Received
September 11, 1984
Decision Date
November 29, 1984
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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Other Clearances by Biotron , Ltd.

K Number Device Name
K910135 THE UNIVERSAL CEMENT PLUG(TM)
K810634 FIRM-A-TRON
K780802 ARMTROL AND FERMTROL
K780803 TILL-U-TEST, DIP SLIDE