RAYTEL DIGITAL IMAGING SYSTEMS
K-Number: K922164 · 1993-01-21
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Device Summary
Frequently Asked Questions
What is the RAYTEL DIGITAL IMAGING SYSTEMS?
RAYTEL DIGITAL IMAGING SYSTEMS is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Olicon Imaging Systems, Inc.. The 510(k) number is K922164.
When did RAYTEL DIGITAL IMAGING SYSTEMS receive FDA 510(k) clearance?
RAYTEL DIGITAL IMAGING SYSTEMS received FDA 510(k) clearance on 1993-01-21, under 510(k) number K922164.
Who is the listed applicant for RAYTEL DIGITAL IMAGING SYSTEMS?
The FDA 510(k) record lists Olicon Imaging Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAYTEL DIGITAL IMAGING SYSTEMS?
The FDA product code for RAYTEL DIGITAL IMAGING SYSTEMS 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 Olicon Imaging Systems, 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.
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