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

LUXOR PORCELAIN

K Number: K820057 · Decision Mar 2, 1982
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
25
Review Days
50

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LUXOR PORCELAIN
K Number
K820057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Jeneric Ind.
Date Received
January 11, 1982
Decision Date
March 2, 1982
Product Code
EIH
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
EIH Powder, Porcelain

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EIH), ordered by most recent decision date.

View all

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
K840563 RX C & B 20
K840561 RX ELAN
K840562 REX V
K834560 VITEX P.D.A
K833774 NATURELLE II & LITE II-N72-N74-L
Search all 25 clearances from Jeneric Ind. →