CHIN UP

Support, Patient Position

EDWARD CARDEN

The following data is part of a premarket notification filed by Edward Carden with the FDA for Chin Up.

Pre-market Notification Details

• Device ID: K943837
• 510k Number: K943837
• Device Name: CHIN UP
• Classification: Support, Patient Position
• Applicant: EDWARD CARDEN 4 JIB ST. #14 Marina Del Rey, CA 90292
• Contact: Edward Hardy
• Correspondent: Edward Hardy; EDWARD CARDEN 4 JIB ST. #14 Marina Del Rey, CA 90292
• Product Code: CCX
• CFR Regulation Number: 868.6820 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1994-08-05
• Decision Date: 1994-10-14