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Clik-FIX PCK-1011

by Starboard Medical, Inc.

Clik-FIX PCK-1011 is a peripheral intravenous catheterization support kit (FDA Class II; FDA product code LRS, I.V. Start Kit) made by Starboard Medical, Inc., listed in FDA GUDID since 8 Mar 2019 (UDI-DI 10850933007242), 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 Number10850933007242 UDI-DI Date8 Mar 2019ListedStatusListed 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  • Withdrawn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
Clik-FIX
Generic name
Peripheral intravenous catheterization support kit
Model / Ref / Catalog
PCK-1011
Primary DI / UDI-DI
10850933007242
FDA product code
LRS
GMDN term
Peripheral intravenous catheterization support kit
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRS (I.V. Start Kit).

Other devices from Starboard Medical, Inc.

See all devices from Starboard Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)