VIVID, MODELS 40-A0001, 40-A0004, 40-A0006
K-Number: K090079 · 2009-05-01
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Device Summary
Frequently Asked Questions
What is the VIVID, MODELS 40-A0001, 40-A0004, 40-A0006?
VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 is a medical device that received FDA 510(k) clearance on 2009-05-01. The listed applicant is Progeny, Inc.. The 510(k) number is K090079.
When did VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 receive FDA 510(k) clearance?
VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 received FDA 510(k) clearance on 2009-05-01, under 510(k) number K090079.
Who is the listed applicant for VIVID, MODELS 40-A0001, 40-A0004, 40-A0006?
The FDA 510(k) record lists Progeny, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIVID, MODELS 40-A0001, 40-A0004, 40-A0006?
The FDA product code for VIVID, MODELS 40-A0001, 40-A0004, 40-A0006 is EIA.
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 Progeny, 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: EIA)
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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