PREVIEW TELEIMAGING SYSTEM
K-Number: K950699 · 1995-05-03
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Device Summary
Frequently Asked Questions
What is the PREVIEW TELEIMAGING SYSTEM?
PREVIEW TELEIMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-05-03. The listed applicant is Regulatory Management Services. The 510(k) number is K950699.
When did PREVIEW TELEIMAGING SYSTEM receive FDA 510(k) clearance?
PREVIEW TELEIMAGING SYSTEM received FDA 510(k) clearance on 1995-05-03, under 510(k) number K950699.
Who is the listed applicant for PREVIEW TELEIMAGING SYSTEM?
The FDA 510(k) record lists Regulatory Management Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREVIEW TELEIMAGING SYSTEM?
The FDA product code for PREVIEW TELEIMAGING SYSTEM 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 Regulatory Management Services 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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