VITALOGRAPH BASE STATION
K-Number: K000599 · 2000-09-08
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Device Summary
Frequently Asked Questions
What is the VITALOGRAPH BASE STATION?
VITALOGRAPH BASE STATION is a medical device that received FDA 510(k) clearance on 2000-09-08. The listed applicant is Vitalograph, Inc.. The 510(k) number is K000599.
When did VITALOGRAPH BASE STATION receive FDA 510(k) clearance?
VITALOGRAPH BASE STATION received FDA 510(k) clearance on 2000-09-08, under 510(k) number K000599.
Who is the listed applicant for VITALOGRAPH BASE STATION?
The FDA 510(k) record lists Vitalograph, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITALOGRAPH BASE STATION?
The FDA product code for VITALOGRAPH BASE STATION is BZG.
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 Vitalograph, 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: BZG)
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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