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Accu-Read BP00-2101

by Reprocessing Products Corp

Accu-Read BP00-2101 is a Class II device made by Reprocessing Products Corp, cleared under FDA 510(k) K171889 on 19 Dec 2017 and listed in FDA GUDID since 29 Aug 2019 (UDI-DI 00858293006434), active as of 22 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 22 Oct 2026

Documents

510(k) K171889

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858293006434 UDI-DI Date29 Aug 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK171889 Date19 Dec 2017DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K171889 decided 19 Dec 2017 Active
  • FDA GUDID UDI-DI 00858293006434 listed 29 Aug 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K171889
  2. Listed FDA GUDID 00858293006434

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Accu-Read
Generic name
Blood pressure cuff, reusable
Model / reference
BP00-2101
Description
BP Cuff, Adult Large, 1 Tube BP00-2105 = 5 pack BP00-2120 = 20 pack
Primary DI / UDI-DI
00858293006434
510(k) Number
FDA product code
DXQ
GMDN term
Blood pressure cuff, reusable
Device class
Class II
Regulation number
870.1120
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DXQ (Blood Pressure Cuff).

Other devices from Reprocessing Products Corp

See all devices from Reprocessing Products Corp →

Properties

  • Lot / batch number
Other properties (14, all answered No)