PHOENIX

Unit, Electrosurgical, Endoscopic (with Or Without Accessories)

MEDICAL AND SCIENTIFIC ENTERPRISES, INC.

The following data is part of a premarket notification filed by Medical And Scientific Enterprises, Inc. with the FDA for Phoenix.

Pre-market Notification Details

• Device ID: K895855
• 510k Number: K895855
• Device Name: PHOENIX
• Classification: Unit, Electrosurgical, Endoscopic (with Or Without Accessories)
• Applicant: MEDICAL AND SCIENTIFIC ENTERPRISES, INC. 29 WALL ST. Foxboro, MA 02035
• Contact: Paul Nardella
• Correspondent: Paul Nardella; MEDICAL AND SCIENTIFIC ENTERPRISES, INC. 29 WALL ST. Foxboro, MA 02035
• Product Code: KNS
• CFR Regulation Number: 876.4300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1989-10-02
• Decision Date: 1990-01-22