VITALOGIK MODEL 4000/4500
K-Number: K073140 · 2007-11-21
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Device Summary
Frequently Asked Questions
What is the VITALOGIK MODEL 4000/4500?
VITALOGIK MODEL 4000/4500 is a medical device that received FDA 510(k) clearance on 2007-11-21. The listed applicant is Mennen Medical , Ltd.. The 510(k) number is K073140.
When did VITALOGIK MODEL 4000/4500 receive FDA 510(k) clearance?
VITALOGIK MODEL 4000/4500 received FDA 510(k) clearance on 2007-11-21, under 510(k) number K073140.
Who is the listed applicant for VITALOGIK MODEL 4000/4500?
The FDA 510(k) record lists Mennen Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITALOGIK MODEL 4000/4500?
The FDA product code for VITALOGIK MODEL 4000/4500 is DSI.
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 Mennen Medical , Ltd. 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: DSI)
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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