FDA 510(k)

ELVI BICLOT 816

K-Number: K812906 · 1982-07-22

Decision Date1982-07-22

Product CodeKQG

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

ELVI BICLOT 816 is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K812906. The device is classified under product code KQG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI BICLOT 816?

ELVI BICLOT 816 is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K812906.

When did ELVI BICLOT 816 receive FDA 510(k) clearance?

ELVI BICLOT 816 received FDA 510(k) clearance on 1982-07-22, under 510(k) number K812906.

Who is the listed applicant for ELVI BICLOT 816?

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 BICLOT 816?

The FDA product code for ELVI BICLOT 816 is KQG.

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Other records listing Volu Sol Medical Industries as applicant

K822128VOLU-SOL SINGLE DIFFERENTIAL STAIN K822127VOLU-SOL ZENKERS FIXATIVE K822126VOLU-SOL CARNOY FLUID K822129VOLU-SOL BOVINS FIXATIVE K822036VOLU-SOL DECALCIFER K822035VOLU-SOL GILLS EA

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Related Devices (Code: KQG)

K050821COAGCARE ANTICOAGULATION MANAGEMENT SYSTEMZycare K021976FIBRON-1, FIBRON-4, QUIKCOAG, FIBRONVital Scientific N.V.K992130PACIFIC HEMOSTASIS THROMBOSCREEN 400CPacific Hemostasis K991321PACIFIC HEMOSTASIS THROMBOSCREEN 200Pacific Hemostasis K983475HEMOCHRON RESPONSEInternational Technidyne Corp.K902614ELVI 828 DIGICLOT MULTISCANLogos Scientific, Inc.

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.