# Home Access A1C Test 84

> Listed: FDA GUDID listing, no authorization on record. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/home-access-a1c-test-84>
- Manufacturer: [Home Access Health Corporation](https://devicerts.com/manufacturers/home-access-health-corporation) (FDA registration: United States)
- Name in the registry: HOME ACCESS A1C TEST 84
- GMDN: Capillary blood collection set, home-use (38092)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI M769A1CPCP841 · listed 2017-10-06 · status: Listed (GUDID: in commercial distribution)

## Recalls

No recall on record.

## Identity

- Trade name: HOME ACCESS A1C TEST [FDA GUDID (AccessGUDID)]
- Generic name: Capillary blood collection set, home-use [FDA GUDID (AccessGUDID)]
- Model / reference: 84 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: M769A1CPCP841 [FDA GUDID (AccessGUDID)]
- GMDN term: Capillary blood collection set, home-use (38092) [FDA GUDID (AccessGUDID)]

## Classification

- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Over-the-counter: Yes [FDA GUDID (AccessGUDID)]
- Convenience kit: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Home Access A1C Test 84, Home Access Health Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/home-access-a1c-test-84 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-11-08
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/home-access-a1c-test-84.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/home-access-a1c-test-84
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.