SNARE

Snare, Flexible

LIGHTHOUSE MEDICAL, INC.

The following data is part of a premarket notification filed by Lighthouse Medical, Inc. with the FDA for Snare.

Pre-market Notification Details

• Device ID: K960230
• 510k Number: K960230
• Device Name: SNARE
• Classification: Snare, Flexible
• Applicant: LIGHTHOUSE MEDICAL, INC. 100 BEAVER ST. Waltham, MA 02154
• Contact: Jenna Andelman
• Correspondent: Jenna Andelman; LIGHTHOUSE MEDICAL, INC. 100 BEAVER ST. Waltham, MA 02154
• Product Code: FDI
• CFR Regulation Number: 876.4300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-01-17
• Decision Date: 1996-07-31