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FDA 510(k)

AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM

K-Number: K934124 · 1994-04-13

ApplicantAndronic Devices, Ltd.
Decision Date1994-04-13
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Andronic Devices, Ltd.. It received FDA 510(k) clearance on 1994-04-13 under 510(k) number K934124. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM?

AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-13. The listed applicant is Andronic Devices, Ltd.. The 510(k) number is K934124.

When did AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM receive FDA 510(k) clearance?

AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM received FDA 510(k) clearance on 1994-04-13, under 510(k) number K934124.

Who is the listed applicant for AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM?

The FDA 510(k) record lists Andronic Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM?

The FDA product code for AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM is JQW.

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Other records listing Andronic Devices, Ltd. 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.

K940812INSIGHT ELECTRONIC ALIGNMENT INDICATORK934928INSITE FILTER & TUBING SETK934926INSITE MODEL 20 & MODEL 15 INSUFFLATORSK935381KAPS POSITIONING ARMK936308ENDEX ENDOSCOPIC POSITIONING SYSTEMK932253ARTHROBOT BI-FOLD DRAPE

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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