MITRA IMAGING INC. EXHIBIT
K-Number: K982769 · 1998-11-03
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Device Summary
Frequently Asked Questions
What is the MITRA IMAGING INC. EXHIBIT?
MITRA IMAGING INC. EXHIBIT is a medical device that received FDA 510(k) clearance on 1998-11-03. The listed applicant is Mitra Imaging, Inc.. The 510(k) number is K982769.
When did MITRA IMAGING INC. EXHIBIT receive FDA 510(k) clearance?
MITRA IMAGING INC. EXHIBIT received FDA 510(k) clearance on 1998-11-03, under 510(k) number K982769.
Who is the listed applicant for MITRA IMAGING INC. EXHIBIT?
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. EXHIBIT?
The FDA product code for MITRA IMAGING INC. EXHIBIT is LLZ.
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: LLZ)
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.
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