picoAMH ELISA— 510(k) DEN180004

Unknown

Ansh Labs, LLC

FDA 510(k) clearance DEN180004 for picoAMH ELISA, Unknown on 2018-10-24. Applicant: Ansh Labs, LLC. Device class: 2.

Clearance details

Applicant
Ansh Labs, LLC
Product code
Code QDH
Device class
Class 2
Regulation
21 CFR 862.1093
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Unknown
Clearance type
Direct
Location
Webster, TX, US
View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.