VORTECH'S MEDICAL IMAGING GATEWAY
K-Number: K884434 · 1989-01-19
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Device Summary
Frequently Asked Questions
What is the VORTECH'S MEDICAL IMAGING GATEWAY?
VORTECH'S MEDICAL IMAGING GATEWAY is a medical device that received FDA 510(k) clearance on 1989-01-19. The listed applicant is Vortech Data, Inc.. The 510(k) number is K884434.
When did VORTECH'S MEDICAL IMAGING GATEWAY receive FDA 510(k) clearance?
VORTECH'S MEDICAL IMAGING GATEWAY received FDA 510(k) clearance on 1989-01-19, under 510(k) number K884434.
Who is the listed applicant for VORTECH'S MEDICAL IMAGING GATEWAY?
The FDA 510(k) record lists Vortech Data, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VORTECH'S MEDICAL IMAGING GATEWAY?
The FDA product code for VORTECH'S MEDICAL IMAGING GATEWAY 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 Vortech Data, 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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