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

SIGNUM

K Number: K001360 · Decision Jun 20, 2000
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
55
Review Days
53

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Basic Information

Device Name
SIGNUM
K Number
K001360
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
J.F. Jelenko & Co., Inc.
Date Received
April 28, 2000
Decision Date
June 20, 2000
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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Other Clearances by J.F. Jelenko & Co., Inc.

K Number Device Name
K012303 JEL-20
K002993 HERACERAM
K002645 JEL BIOS PURE
K002222 RD-2104
K001260 ALLROUND 55 LF
K001196 JEL BIOS 90 (CODE NAME RD-2401)
K000532 JEL 15
K993136 JEL BIOS 10 (CODE NAME RD-1801)
K993152 JEL BIOS 18 (CODE NAME RD- 1214)
K991564 JELTEMP
Search all 55 clearances from J.F. Jelenko & Co., Inc. →