MOLYBDENUM

Assembly, Tube Housing, X-ray, Diagnostic

SOUTHEASTERN MEDICAL DIAGNOSTICS, INC.

The following data is part of a premarket notification filed by Southeastern Medical Diagnostics, Inc. with the FDA for Molybdenum.

Pre-market Notification Details

• Device ID: K923094
• 510k Number: K923094
• Device Name: MOLYBDENUM
• Classification: Assembly, Tube Housing, X-ray, Diagnostic
• Applicant: SOUTHEASTERN MEDICAL DIAGNOSTICS, INC. P.O. BOX 10173 Greensboro, NC 27404
• Contact: Peter Gratale
• Correspondent: Peter Gratale; SOUTHEASTERN MEDICAL DIAGNOSTICS, INC. P.O. BOX 10173 Greensboro, NC 27404
• Product Code: ITY
• CFR Regulation Number: 892.1760 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-06-25
• Decision Date: 1993-03-04