PRINCE

Alloy, Amalgam

GOLDSMITH & REVERE, INC.

The following data is part of a premarket notification filed by Goldsmith & Revere, Inc. with the FDA for Prince.

Pre-market Notification Details

• Device ID: K933309
• 510k Number: K933309
• Device Name: PRINCE
• Classification: Alloy, Amalgam
• Applicant: GOLDSMITH & REVERE, INC. 242 S. DEAN ST. Englewood, NJ 07631
• Contact: Tim Wolf
• Correspondent: Tim Wolf; GOLDSMITH & REVERE, INC. 242 S. DEAN ST. Englewood, NJ 07631
• Product Code: EJJ
• CFR Regulation Number: 872.3070 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-07-07
• Decision Date: 1993-10-01