ELVI 840 AGGREGOMETER
K-Number: K791577 · 1979-09-17
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Device Summary
Frequently Asked Questions
What is the ELVI 840 AGGREGOMETER?
ELVI 840 AGGREGOMETER is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K791577.
When did ELVI 840 AGGREGOMETER receive FDA 510(k) clearance?
ELVI 840 AGGREGOMETER received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791577.
Who is the listed applicant for ELVI 840 AGGREGOMETER?
The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELVI 840 AGGREGOMETER?
The FDA product code for ELVI 840 AGGREGOMETER is JOZ.
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 Volu Sol Medical Industries 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: JOZ)
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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