TELEVISIT

Oximeter

PHD MEDICAL

The following data is part of a premarket notification filed by Phd Medical with the FDA for Televisit.

Pre-market Notification Details

• Device ID: K062338
• 510k Number: K062338
• Device Name: TELEVISIT
• Classification: Oximeter
• Applicant: PHD MEDICAL 4 INNOVATION DRIVE Dundas, On, CA L9h 7p3
• Contact: Nancy Ruth
• Correspondent: Nancy Ruth; PHD MEDICAL 4 INNOVATION DRIVE Dundas, On, CA L9h 7p3
• Product Code: DQA
• CFR Regulation Number: 870.2700 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2006-08-10
• Decision Date: 2006-10-25
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00628250477016	K062338	000