PEEPER

Attachment, Breathing, Positive End Expiratory Pressure

DUPACO, INC.

The following data is part of a premarket notification filed by Dupaco, Inc. with the FDA for Peeper.

Pre-market Notification Details

• Device ID: K830395
• 510k Number: K830395
• Device Name: PEEPER
• Classification: Attachment, Breathing, Positive End Expiratory Pressure
• Applicant: DUPACO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: BYE
• CFR Regulation Number: 868.5965 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-02-07
• Decision Date: 1983-03-11