AUTOPRIME

Filter, Infusion Line

ARBOR TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Arbor Technologies, Inc. with the FDA for Autoprime.

Pre-market Notification Details

• Device ID: K964283
• 510k Number: K964283
• Device Name: AUTOPRIME
• Classification: Filter, Infusion Line
• Applicant: ARBOR TECHNOLOGIES, INC. 401 WEST MORGAN RD. Ann Arbor, MI 48108
• Contact: Dawn I Moore
• Correspondent: Dawn I Moore; ARBOR TECHNOLOGIES, INC. 401 WEST MORGAN RD. Ann Arbor, MI 48108
• Product Code: FPB
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-10-28
• Decision Date: 1997-01-22
• Summary: summary