NITRO

Wheelchair, Mechanical

EVEREST & JENNINGS, INC.

The following data is part of a premarket notification filed by Everest & Jennings, Inc. with the FDA for Nitro.

Pre-market Notification Details

• Device ID: K940304
• 510k Number: K940304
• Device Name: NITRO
• Classification: Wheelchair, Mechanical
• Applicant: EVEREST & JENNINGS, INC. 1100 CORPORATE SQUARE DR. St. Louis, MO 63132
• Contact: Jackie Wilkins
• Correspondent: Jackie Wilkins; EVEREST & JENNINGS, INC. 1100 CORPORATE SQUARE DR. St. Louis, MO 63132
• Product Code: IOR
• CFR Regulation Number: 890.3850 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1994-01-24
• Decision Date: 1994-02-17