GERONIMO

Wheelchair, Powered

REDMAN, INC.

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

Pre-market Notification Details

• Device ID: K935750
• 510k Number: K935750
• Device Name: GERONIMO
• Classification: Wheelchair, Powered
• Applicant: REDMAN, INC. 945 EAST OHIO, SUITE #4 Tucson, AZ 85714
• Contact: Don Redman
• Correspondent: Don Redman; REDMAN, INC. 945 EAST OHIO, SUITE #4 Tucson, AZ 85714
• Product Code: ITI
• CFR Regulation Number: 890.3860 [🔎]
• Decision: Substantially Equivalent For Some Indications (SN)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-11-26
• Decision Date: 1995-02-03