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

RX C & B 20

K Number: K840563 · Decision May 1, 1984
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
193
Applicant Total
25
Review Days
83

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Basic Information

Device Name
RX C & B 20
K Number
K840563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Jeneric Ind.
Date Received
February 8, 1984
Decision Date
May 1, 1984
Product Code
EJS
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EJS Alloy, Other Noble Metal

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Other Clearances by Jeneric Ind.

K Number Device Name
K862822 REXILLIUM N. B. F.
K862926 SURGICAL VITEX
K854878 H40 BASE METAL ALLOY
K844123 RX CBY
K844122 RX CBG
K840561 RX ELAN
K840562 REX V
K834560 VITEX P.D.A
K833774 NATURELLE II & LITE II-N72-N74-L
K833736 GOLD-PALLADIUM-SILVER BASED CAST/ALLOY
Search all 25 clearances from Jeneric Ind. →