CPR SHIELD

Device, Cpr Assist

RONDEX PRODUCTS, INC.

The following data is part of a premarket notification filed by Rondex Products, Inc. with the FDA for Cpr Shield.

Pre-market Notification Details

• Device ID: K942671
• 510k Number: K942671
• Device Name: CPR SHIELD
• Classification: Device, Cpr Assist
• Applicant: RONDEX PRODUCTS, INC. P.O. BOX NO. 1829 Rockford, IL 61110
• Contact: Gene R Baldwin
• Correspondent: Gene R Baldwin; RONDEX PRODUCTS, INC. P.O. BOX NO. 1829 Rockford, IL 61110
• Product Code: LYM
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1994-06-06
• Decision Date: 1995-02-07

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
06343760395509	K942671	000
00634376495575	K942671	000
00634376095577	K942671	000
00634376095003	K942671	000
00634376195574	K942671	000
06343760095003	K942671	000
06343760095072	K942671	000
06343760095508	K942671	000
06343760095577	K942671	000
06343760195574	K942671	000
06343760295571	K942671	000
00634376495506	K942671	000