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CloudCover NL-SK-5S

by Neolight LLC

CloudCover NL-SK-5S is a blanket/pad infant phototherapy unit (FDA Class II; FDA product code LBI, Unit, Neonatal Phototherapy) made by Neolight LLC, cleared under FDA 510(k) K170585 on 27 Oct 2017 and listed in FDA GUDID since 11 Nov 2020 (UDI-DI 10852788008177), 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) K170585

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 Number10852788008177 UDI-DI Date11 Nov 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK170585 Date27 Oct 2017DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K170585 decided 27 Oct 2017 Active
  • FDA GUDID UDI-DI 10852788008177 listed 11 Nov 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K170585
  2. Listed FDA GUDID 10852788008177

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
CloudCover
Generic name
Blanket/pad infant phototherapy unit
Model / Ref / Catalog
NL-SK-5S
Primary DI / UDI-DI
10852788008177
510(k) Number
FDA product code
LBI
GMDN term
Blanket/pad infant phototherapy unit
Device class
Class II
Regulation number
880.5700
GUDID distribution status
In Commercial Distribution

Other devices from Neolight LLC

See all devices from Neolight LLC →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)