MOVES

Ventilator, Emergency, Powered (resuscitator)

THORNHILL RESEARCH INC

The following data is part of a premarket notification filed by Thornhill Research Inc with the FDA for Moves.

Pre-market Notification Details

• Device ID: K093261
• 510k Number: K093261
• Device Name: MOVES
• Classification: Ventilator, Emergency, Powered (resuscitator)
• Applicant: THORNHILL RESEARCH INC 70 PETER ST. 2ND FL. Toronto, Ontario, CA M5v 2g5
• Contact: Cliff Ansel
• Correspondent: Cliff Ansel; THORNHILL RESEARCH INC 70 PETER ST. 2ND FL. Toronto, Ontario, CA M5v 2g5
• Product Code: BTL
• CFR Regulation Number: 868.5925 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2009-10-19
• Decision Date: 2010-03-26
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
18071411242418	K093261	000
10807141000152	K093261	000
10807141000145	K093261	000
10807141000138	K093261	000
10807141000084	K093261	000
10807141000077	K093261	000
10807141000060	K093261	000
20807141000050	K093261	000
20807141000036	K093261	000
10807141000015	K093261	000
10807141000169	K093261	000
18071411006263	K093261	000
18071411008168	K093261	000
18071411115590	K093261	000
18071411114227	K093261	000
18071411243538	K093261	000
18071411243521	K093261	000
18071411008236	K093261	000
18071411243507	K093261	000
18071411006959	K093261	000
18071411006270	K093261	000
10807141000008	K093261	000