Skip to content

Home Access A1C Test 84

by Home Access Health Corporation

Home Access A1C Test 84 is a capillary blood collection set made by Home Access Health Corporation, listed in FDA GUDID since 6 Oct 2017 (UDI-DI M769A1CPCP841), registry data as of 8 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM769A1CPCP841 UDI-DI Date6 Oct 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Home Access A1C Test
Generic name
Capillary blood collection set, home-use
Model / reference
84
Primary DI / UDI-DI
M769A1CPCP841
GMDN term
Capillary blood collection set, home-use
GUDID distribution status
In Commercial Distribution

Related devices

Category: Capillary blood collection set, home-use

Other devices from Home Access Health Corporation

See all devices from Home Access Health Corporation →

Properties

  • Single use
  • Prescription use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)