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Aneroids (82 etc.) 82-PPK

by Rashman Corp.

Aneroids (82 etc.) 82-PPK is a Class II device made by Rashman Corp., cleared under FDA 510(k) K082542 on 17 Sep 2008 and listed in FDA GUDID since 1 Sep 2022 (UDI-DI 00786511412807), 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) K082542

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 Number00786511412807 UDI-DI Date1 Sep 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK082542 Date17 Sep 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K082542 decided 17 Sep 2008 Active
  • FDA GUDID UDI-DI 00786511412807 listed 1 Sep 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K082542
  2. Listed FDA GUDID 00786511412807

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Aneroids (82 etc.)
Generic name
Aneroid manual sphygmomanometer
Model / reference
82-PPK
Primary DI / UDI-DI
00786511412807
510(k) Number
FDA product code
DXQ
GMDN term
Aneroid manual sphygmomanometer
Device class
Class II
Regulation number
870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometer

Cleared under the same submission (K082542)

and 8 more cleared under K082542

Similar devices

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

Other devices from Rashman Corp.

See all devices from Rashman Corp. →

Properties

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