FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

DEKA LOTUS

K Number: K250281 · Decision Feb 26, 2025
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
73
Applicant Total
15
Review Days
26

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Basic Information

Device Name
DEKA LOTUS
K Number
K250281
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
El.En S.P.A.
Date Received
January 31, 2025
Decision Date
February 26, 2025
Product Code
ONF
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Similar 510(k) Clearances

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

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Other Clearances by El.En S.P.A.

K Number Device Name
K260647 SPECCHIO
K251432 Olo
K243683 Deka Bluebeam
K241459 MOTUS PRO Family
K240752 DEKA TORO
K233473 DEKA LOTUS
K234057 NIRVANA
K240537 SMARTXIDE PRO
K240497 Smartxide Tetra Pro
K233470 DEKA LILY
Search all 15 clearances from El.En S.P.A. →