RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,

Wheelchair, Mechanical

CONVAID PRODUCTS, INC.

The following data is part of a premarket notification filed by Convaid Products, Inc. with the FDA for Rodeo Model, Rd12, Rd14, Rd16, Radio Transit Model, Rd12t, Rd14t, Rd16t,.

Pre-market Notification Details

• Device ID: K032402
• 510k Number: K032402
• Device Name: RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,
• Classification: Wheelchair, Mechanical
• Applicant: CONVAID PRODUCTS, INC. 2830 CALIFORNIA ST. Torrance, CA 90503
• Contact: Donald Griggs
• Correspondent: Donald Griggs; CONVAID PRODUCTS, INC. 2830 CALIFORNIA ST. Torrance, CA 90503
• Product Code: IOR
• CFR Regulation Number: 890.3850 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2003-08-04
• Decision Date: 2003-09-24
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10840117400198	K032402	000
10840117400242	K032402	000
10840117400259	K032402	000
10840117400266	K032402	000
10840117400273	K032402	000
10840117400303	K032402	000
10840117400310	K032402	000
10840117401478	K032402	000
10840117401485	K032402	000
10840117401751	K032402	000
10840117403311	K032402	000
10840117405803	K032402	000
10840117405810	K032402	000
10840117405827	K032402	000
10840117405834	K032402	000
10840117400228	K032402	000