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hsCRP CAL CP2478

by Randox Laboratories, Ltd.

hsCRP CAL CP2478 is a Class II device made by Randox Laboratories, Ltd., cleared under FDA 510(k) K022682 on 5 Nov 2002 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05055273201680), active as of 22 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 22 Oct 2026

Documents

510(k) K022682

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055273201680 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK022682 Date5 Nov 2002DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K022682 decided 5 Nov 2002 Active
  • FDA GUDID UDI-DI 05055273201680 listed 16 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K022682
  2. Listed FDA GUDID 05055273201680

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
hsCRP CAL
Generic name
C-reactive protein (CRP) IVD, calibrator
Model / Ref / Catalog
CP2478
Primary DI / UDI-DI
05055273201680
510(k) Number
FDA product code
JIS
GMDN term
C-reactive protein (CRP) IVD, calibrator
Device class
Class II
Regulation number
862.1150
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under C-reactive protein (CRP) IVD, calibrator.

Other devices from Randox Laboratories, Ltd.

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Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)