T3 UPTAKE TEST

Radioassay, Triiodothyronine Uptake

MONOBIND

The following data is part of a premarket notification filed by Monobind with the FDA for T3 Uptake Test.

Pre-market Notification Details

• Device ID: K780361
• 510k Number: K780361
• Device Name: T3 UPTAKE TEST
• Classification: Radioassay, Triiodothyronine Uptake
• Applicant: MONOBIND 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: KHQ
• CFR Regulation Number: 862.1715 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1978-03-06
• Decision Date: 1978-03-22

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00840239032676	K780361	000