EZ PUMP

Scale, Patient

ALPHAMED, INC.

The following data is part of a premarket notification filed by Alphamed, Inc. with the FDA for Ez Pump.

Pre-market Notification Details

• Device ID: K926446
• 510k Number: K926446
• Device Name: EZ PUMP
• Classification: Scale, Patient
• Applicant: ALPHAMED, INC. POST OFFICE BOX 550 Duluth, GA 30136
• Contact: David Ammann
• Correspondent: David Ammann; ALPHAMED, INC. POST OFFICE BOX 550 Duluth, GA 30136
• Product Code: FRW
• CFR Regulation Number: 880.2720 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-12-23
• Decision Date: 1993-09-27