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PowerLook 9.1

by Icad, Inc.

PowerLook 9.1 is a Class I device made by Icad, Inc., listed in FDA GUDID since 11 Jul 2019 (UDI-DI 00858012005977), registry data as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858012005977 UDI-DI Date11 Jul 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
PowerLook
Generic name
Radiology DICOM image processing application software
Model / reference
9.1
Primary DI / UDI-DI
00858012005977
FDA product code
LMD
GMDN term
Radiology DICOM image processing application software
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)