THINQ

System, Image Processing, Radiological

CorticoMetrics LLC

The following data is part of a premarket notification filed by Corticometrics Llc with the FDA for Thinq.

Pre-market Notification Details

• Device ID: K192051
• 510k Number: K192051
• Device Name: THINQ
• Classification: System, Image Processing, Radiological
• Applicant: CorticoMetrics LLC 128 Granite St. Rockport, MA 01966
• Contact: Nick Schmansky
• Correspondent: Nick Schmansky; CorticoMetrics LLC 128 Granite St. Rockport, MA 01966
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2019-07-31
• Decision Date: 2020-09-30

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
B801THINQ1000	K192051	000
B801THINQ1130	K192051	000