TEMP TRACE

Thermometer, Electronic, Clinical

PROGRESS MANKIND TECHNOLOGY

The following data is part of a premarket notification filed by Progress Mankind Technology with the FDA for Temp Trace.

Pre-market Notification Details

• Device ID: K830530
• 510k Number: K830530
• Device Name: TEMP TRACE
• Classification: Thermometer, Electronic, Clinical
• Applicant: PROGRESS MANKIND TECHNOLOGY 4221 Richmond Rd., N.W. Walker, MI 49534
• Product Code: FLL
• CFR Regulation Number: 880.2910 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-02-18
• Decision Date: 1983-04-06

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10650551046339	K830530	000
10650551046322	K830530	000