Skip to content

ClearRead +Detect 5.2.3

by Riverain Technologies, Inc. 11 variants

ClearRead +Detect 5.2.3, a radiological PACS-dedicated management software (FDA Class II; FDA product code MYN, Analyzer,Medical Image) made by Riverain Technologies, Inc., was listed in FDA GUDID on 9 Mar 2016 (UDI-DI M722C16033C160130); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM722C16033C160130 UDI-DI Date9 Mar 2016ListedStatusListed GUDID: not 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  • Withdrawn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
ClearRead +Detect
Generic name
Radiological PACS-dedicated management software
Model / reference
5.2.3
Primary DI / UDI-DI
M722C16033C160130
FDA product code
MYN
GMDN term
Radiological PACS-dedicated management software
Device class
Class II
Regulation number
892.2070
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code MYN (Analyzer,Medical Image).

Other devices from Riverain Technologies, Inc.

See all devices from Riverain Technologies, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)