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Immco Diagnostics 2302-60

by Immco Diagnostics, Inc.

Immco Diagnostics 2302-60 is a Class II device made by Immco Diagnostics, Inc., cleared under FDA 510(k) K883949 on 27 Oct 1988 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00845714004339), 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) K883949

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 Number00845714004339 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK883949 Date27 Oct 1988DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K883949 decided 27 Oct 1988 Active
  • FDA GUDID UDI-DI 00845714004339 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K883949
  2. Listed FDA GUDID 00845714004339

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  • Withdrawn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
Buffered sample diluent IVD
Model / Ref / Catalog
2302-60
Primary DI / UDI-DI
00845714004339
510(k) Number
FDA product code
LKJ
GMDN term
Buffered sample diluent IVD
Device class
Class II
Regulation number
866.5100
GUDID distribution status
In Commercial Distribution

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Properties

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