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Cyber Blade 20049001

by Sidam SRL

Cyber Blade 20049001 is a Class II device made by Sidam SRL, cleared under FDA 510(k) K192499 on 31 Jul 2020 and listed in FDA GUDID since 4 Feb 2021 (UDI-DI 08051414960482), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K192499

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08051414960482 UDI-DI Date4 Feb 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK192499 Date31 Jul 2020DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K192499 decided 31 Jul 2020 Active
  • FDA GUDID UDI-DI 08051414960482 listed 4 Feb 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K192499
  2. Listed FDA GUDID 08051414960482

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Cyber Blade
Generic name
Noninvasive device battery charger
Model / reference
20049001
Primary DI / UDI-DI
08051414960482
510(k) Number
FDA product code
GCJ
GMDN term
Noninvasive device battery charger
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GCJ (Laparoscope, General & Plastic Surgery).

Other devices from Sidam SRL

  • Cyber Blade 20041001

    Class II
  • Cyber Blade 20042001

    Class II

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)