ALARM

Pump, Infusion

MADDAK, INC.

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

Pre-market Notification Details

• Device ID: K790559
• 510k Number: K790559
• Device Name: ALARM
• Classification: Pump, Infusion
• Applicant: MADDAK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: FRN
• CFR Regulation Number: 880.5725 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-03-19
• Decision Date: 1979-06-01