NON-INVASIVE CLINICAL VASCULAR LAB
K-Number: K832679 · 1984-01-03
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Device Summary
Frequently Asked Questions
What is the NON-INVASIVE CLINICAL VASCULAR LAB?
NON-INVASIVE CLINICAL VASCULAR LAB is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K832679.
When did NON-INVASIVE CLINICAL VASCULAR LAB receive FDA 510(k) clearance?
NON-INVASIVE CLINICAL VASCULAR LAB received FDA 510(k) clearance on 1984-01-03, under 510(k) number K832679.
Who is the listed applicant for NON-INVASIVE CLINICAL VASCULAR LAB?
The FDA 510(k) record lists Life Sciences Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-INVASIVE CLINICAL VASCULAR LAB?
The FDA product code for NON-INVASIVE CLINICAL VASCULAR LAB is DQC.
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 Life Sciences Manufacturing, 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: DQC)
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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