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Skytron 5-010-16

by Skytron, LLC

Skytron 5-010-16 is a fluoroscopy/angiography table top (FDA Class I; FDA product code FQO, Table, Operating-Room, Ac-Powered) made by Skytron, LLC, listed in FDA GUDID since 29 Jan 2022 (UDI-DI 10841736122775), 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 Number10841736122775 UDI-DI Date29 Jan 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Skytron
Generic name
Fluoroscopy/angiography table top
Model / Ref / Catalog
5-010-16
Primary DI / UDI-DI
10841736122775
FDA product code
FQO
GMDN term
Fluoroscopy/angiography table top
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FQO (TABLE, OPERATING-ROOM, AC-POWERED).

Other devices from Skytron, LLC

See all devices from Skytron, LLC →

Properties

  • Over-the-counter
  • Convenience kit
  • Premarket exempt
Other properties (12, all answered No)