MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE
K-Number: K970652 · 1997-05-02
Advertisement
Device Summary
Frequently Asked Questions
What is the MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE?
MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE is a medical device that received FDA 510(k) clearance on 1997-05-02. The listed applicant is Mitra Imaging, Inc.. The 510(k) number is K970652.
When did MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE receive FDA 510(k) clearance?
MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE received FDA 510(k) clearance on 1997-05-02, under 510(k) number K970652.
Who is the listed applicant for MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE?
The FDA 510(k) record lists Mitra Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE?
The FDA product code for MITRA IMAGING, INC. FILM EXPRESS SCANNING SOFTWARE is LMD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Mitra Imaging, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LMD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement