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Immco Diagnostic 2510

by Immco Diagnostics, Inc.

Immco Diagnostic 2510 is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K060157 on 25 May 2006 (9 earlier submissions) and listed in FDA GUDID since 27 Oct 2016 (UDI-DI 00845714004186), 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

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845714004186 UDI-DI Date27 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK060157 Date25 May 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K060157 decided 25 May 2006 Active· +9 more in the status table
  • FDA GUDID UDI-DI 00845714004186 listed 27 Oct 2016 Listed

Timeline

11 dated events

  1. Cleared FDA 510(k) K883883
  2. Cleared FDA 510(k) K883949
  3. Cleared FDA 510(k) K884400
  4. Cleared FDA 510(k) K891098
  5. Cleared FDA 510(k) K891099
  6. Cleared FDA 510(k) K912551
  7. Cleared FDA 510(k) K913360
  8. Cleared FDA 510(k) K982898
  9. Cleared FDA 510(k) K060157
  10. Listed FDA GUDID 00845714004186

1 earlier event are in the sections above.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Immco Diagnostic
Generic name
Evans blue solution IVD
Model / Ref / Catalog
2510
Primary DI / UDI-DI
00845714004186
510(k) Number
FDA product code
DBL, LKJ, MOB, DHN
GMDN term
Evans blue solution IVD
Device class
Class II
Regulation number
866.5660, 866.5100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Evans blue solution IVD

Cleared under the same submission (K060157)

and 8 more cleared under K060157

Cleared under the same submission (K883883)

and 8 more cleared under K883883

Similar devices

Other devices filed under FDA product code DBL (Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control).

Other devices from Immco Diagnostics, Inc.

See all devices from Immco Diagnostics, Inc. →

Properties

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