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ANA Negative Control ANN-1010

by Bion Enterprises, Ltd.

ANA Negative Control ANN-1010 is a Class II device made by Bion Enterprises, Ltd., cleared under FDA 510(k) K872845 on 17 Aug 1987 and listed in FDA GUDID since 12 Sep 2016 (UDI-DI B110ANN10100), 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) K872845

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 NumberB110ANN10100 UDI-DI Date12 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK872845 Date17 Aug 1987DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K872845 decided 17 Aug 1987 Active
  • FDA GUDID UDI-DI B110ANN10100 listed 12 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K872845
  2. Listed FDA GUDID B110ANN10100

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
ANA Negative Control
Generic name
Multiple antinuclear antibody (ANA) IVD, control
Model / Ref / Catalog
ANN-1010
Primary DI / UDI-DI
B110ANN10100
510(k) Number
FDA product code
DHN
GMDN term
Multiple antinuclear antibody (ANA) IVD, control
Device class
Class II
Regulation number
866.5100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DHN (Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control).

Other devices from Bion Enterprises, Ltd.

See all devices from Bion Enterprises, Ltd. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)