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Mission Cholesterol Test Device - 3-in-1 Lipid Panel 25T C131-2041

by Acon Laboratories, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00682607690053 UDI-DI Date9 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Mission Cholesterol Test Device - 3-in-1 Lipid Panel 25T
Generic Name
Total cholesterol lipid IVD, kit, spectrophotometry
Model / Ref / Catalog
C131-2041
Primary DI / UDI-DI
00682607690053
510(k) Number
FDA Product Code
LBR, CHH, JGY
GMDN Term
Total cholesterol lipid IVD, kit, spectrophotometry
Device Class
Class I
Regulation Number
862.1475, 862.1175, 862.1705
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K163406)

Other devices from Acon Laboratories, Inc.

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Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No