VITALOGRAPH MICRO
K-Number: K991412 · 2000-02-04
Advertisement
Device Summary
Frequently Asked Questions
What is the VITALOGRAPH MICRO?
VITALOGRAPH MICRO is a medical device that received FDA 510(k) clearance on 2000-02-04. The listed applicant is Vitalograph, Inc.. The 510(k) number is K991412.
When did VITALOGRAPH MICRO receive FDA 510(k) clearance?
VITALOGRAPH MICRO received FDA 510(k) clearance on 2000-02-04, under 510(k) number K991412.
Who is the listed applicant for VITALOGRAPH MICRO?
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 MICRO?
The FDA product code for VITALOGRAPH MICRO is BZH.
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: BZH)
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