Elvi 840 Aggregometer

FDA 510(k) K791577 · Volu Sol Medical Industries

Substantially Equivalent

510(k) numberK791577

Submission

Device name
Elvi 840 Aggregometer
Applicant
Volu Sol Medical Industries
Mchenry, IL, US
Received
August 17, 1979
Decision date
September 17, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOZ – System, Automated Platelet Aggregation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5700
Specialty
Hematology

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K822126Volu-Sol Carnoy FluidIGM · Traditional 08/05/1982SE
K822038Volu-Sol Orange G-6(GILLS-MODHZH · Traditional 08/03/1982SE
K822037Volu-Sol Tap Water SubstitutePPM · Traditional 08/03/1982SE
K822036Volu-Sol DecalciferKDX · Traditional 08/03/1982SE
K822035Volu-Sol Gills EaHZJ · Traditional 08/03/1982SE
K812906Elvi Biclot 816KQG · Traditional 07/22/1982SE
K821541Hematoxylin IIIHYJ · Traditional 06/10/1982SE

Questions and answers

When was Elvi 840 Aggregometer cleared by the FDA?

Elvi 840 Aggregometer (K791577) received a 510(k) decision of Substantially Equivalent on September 17, 1979, 31 days after the submission was received.

What is the product code of K791577?

The FDA product code is JOZ – System, Automated Platelet Aggregation, a Class II (moderate risk) device regulated under 21 CFR 864.5700.