AUTOVAC

Pump, Portable, Aspiration (manual Or Powered)

LIFE SUPPORT PRODUCTS, INC.

The following data is part of a premarket notification filed by Life Support Products, Inc. with the FDA for Autovac.

Pre-market Notification Details

• Device ID: K921107
• 510k Number: K921107
• Device Name: AUTOVAC
• Classification: Pump, Portable, Aspiration (manual Or Powered)
• Applicant: LIFE SUPPORT PRODUCTS, INC. ONE MAUCHLY Irvine, CA 92718
• Contact: Vrnon Trimble
• Correspondent: Vrnon Trimble; LIFE SUPPORT PRODUCTS, INC. ONE MAUCHLY Irvine, CA 92718
• Product Code: BTA
• CFR Regulation Number: 878.4780 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-03-09
• Decision Date: 1992-09-17