FDA 510(k)

PRECISION LIQUID DISPENSER

K-Number: K832205 · 1983-08-24

Decision Date1983-08-24

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

PRECISION LIQUID DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Co.. It received FDA 510(k) clearance on 1983-08-24 under 510(k) number K832205. 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 PRECISION LIQUID DISPENSER?

PRECISION LIQUID DISPENSER is a medical device that received FDA 510(k) clearance on 1983-08-24. The listed applicant is Hamilton Co.. The 510(k) number is K832205.

When did PRECISION LIQUID DISPENSER receive FDA 510(k) clearance?

PRECISION LIQUID DISPENSER received FDA 510(k) clearance on 1983-08-24, under 510(k) number K832205.

Who is the listed applicant for PRECISION LIQUID DISPENSER?

The FDA 510(k) record lists Hamilton Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION LIQUID DISPENSER?

The FDA product code for PRECISION LIQUID DISPENSER is JQW.

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Other records listing Hamilton Co. as applicant

K961896MICROLAB 4000, MICROLAB 4200 K943493DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER K892369MULTI-PROBE HEAD PLUS K873893LUMICON K871945MICROLAB AT K832204MICROLAB P

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Related Devices (Code: JQW)

K023955BD VIPER INSTRUMENTBecton, Dickinson & CO K973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters Corporation K970420MASTERCAP 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.