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CyberLAB 7.3.1

by Aspyra, LLC.

CyberLAB 7.3.1 (CL731) is a Class I device made by Aspyra, LLC., listed in FDA GUDID since 12 Oct 2022 (UDI-DI B433CL0), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB433CL0 UDI-DI Date12 Oct 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
CyberLAB
Generic name
Clinical laboratory information system application software
Model / Ref / Catalog
7.3.1, CL731
Primary DI / UDI-DI
B433CL0
FDA product code
NVV
GMDN term
Clinical laboratory information system application software
Device class
Class I
Regulation number
862.2100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Clinical laboratory information system application software

Other devices from Aspyra, LLC.

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)