VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)
K-Number: K925097 · 1993-01-15
Advertisement
Device Summary
Frequently Asked Questions
What is the VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)?
VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING) is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Vortech Data, Inc.. The 510(k) number is K925097.
When did VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING) receive FDA 510(k) clearance?
VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING) received FDA 510(k) clearance on 1993-01-15, under 510(k) number K925097.
Who is the listed applicant for VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)?
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 AUTOROUTER (AUTOMATIC IMAGE ROUTING)?
The FDA product code for VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING) 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.
Advertisement