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Immco Diagnostics 1102-120X

by Immco Diagnostics, Inc.

Immco Diagnostics 1102-120X is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K883883 on 27 Oct 1988 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00845714000836), 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) K883883

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 Number00845714000836 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK883883 Date27 Oct 1988DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K883883 decided 27 Oct 1988 Active
  • FDA GUDID UDI-DI 00845714000836 listed 21 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K883883
  2. Listed FDA GUDID 00845714000836

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Immco Diagnostics
Generic name
Multiple antinuclear antibody (ANA) IVD, kit, fluorescent immunoassay
Model / Ref / Catalog
1102-120X
Primary DI / UDI-DI
00845714000836
510(k) Number
FDA product code
LKJ
GMDN term
Multiple antinuclear antibody (ANA) IVD, kit, fluorescent immunoassay
Device class
Class II
Regulation number
866.5100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay

Cleared under the same submission (K883883)

and 8 more cleared under K883883

Similar devices in this category

Other devices filed under Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay.

Other devices from Immco Diagnostics, Inc.

See all devices from Immco Diagnostics, Inc. →

Properties

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