• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
1 1

FDA 510(k) K061855, NEUROQUANT, by Cortechs Labs, Inc.

FDA 510(k) K061855, NEUROQUANT, by Cortechs Labs, Inc.

$89.00 USD
$89.00 USD
Sale Sold out
510(K) Number: K061855
Device Name: NEUROQUANT
Manufacturer: Cortechs Labs, Inc.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 06/30/2006
Decision Date: 08/10/2006
Regulation Medical Specialty: Radiology
View full details
FOIA Pro

This drug has a lot more FDA history than one product page can show

FOIA Pro gives you full-text search across 70,000+ FDA FOIA records, from 2020 through today, plus a monthly monitor tracking new requests as they close.
  • Full-text search across every FDA FOIA log since 2020
  • Warning letters, approval records, and correspondence in one place
  • Monthly FDA FOIA Monitor newsletter, included
  • Cancel anytime, monthly or annual billing
Get FOIA Pro
Live search · FOIA database
Searching related FDA records…
ClosedTypeSubjectOutcome