CPROTECTOR

Device, Cpr Assist

CERTIFIED SAFETY MFG., INC.

The following data is part of a premarket notification filed by Certified Safety Mfg., Inc. with the FDA for Cprotector.

Pre-market Notification Details

• Device ID: K934821
• 510k Number: K934821
• Device Name: CPROTECTOR
• Classification: Device, Cpr Assist
• Applicant: CERTIFIED SAFETY MFG., INC. 1400 CHESTNUT Kansas City, MO 64127
• Contact: Howard Gerson
• Correspondent: Howard Gerson; CERTIFIED SAFETY MFG., INC. 1400 CHESTNUT Kansas City, MO 64127
• 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: 1993-10-08
• Decision Date: 1994-01-06