ENDORINGS

Endoscopic Access Overtube, Gastroenterology-urology

ENDO-AID, INC.

The following data is part of a premarket notification filed by Endo-aid, Inc. with the FDA for Endorings.

Pre-market Notification Details

• Device ID: K133359
• 510k Number: K133359
• Device Name: ENDORINGS
• Classification: Endoscopic Access Overtube, Gastroenterology-urology
• Applicant: ENDO-AID, INC. 1835 MARKET STREET, 29TH FLOOR Philadelphia, PA 19103
• Contact: Janice M Hogan
• Correspondent: Janice M Hogan; ENDO-AID, INC. 1835 MARKET STREET, 29TH FLOOR Philadelphia, PA 19103
• Product Code: FED
• CFR Regulation Number: 876.1500 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2013-10-31
• Decision Date: 2014-02-11
• Summary: summary