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FDA 510(k)

KEMBLE LIQUID HANDLING SYSTEM DISPENSER

K-Number: K896684 · 1990-04-16

ApplicantSchiff & Co.
Decision Date1990-04-16
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KEMBLE LIQUID HANDLING SYSTEM DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Schiff & Co.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K896684. 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 KEMBLE LIQUID HANDLING SYSTEM DISPENSER?

KEMBLE LIQUID HANDLING SYSTEM DISPENSER is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Schiff & Co.. The 510(k) number is K896684.

When did KEMBLE LIQUID HANDLING SYSTEM DISPENSER receive FDA 510(k) clearance?

KEMBLE LIQUID HANDLING SYSTEM DISPENSER received FDA 510(k) clearance on 1990-04-16, under 510(k) number K896684.

Who is the listed applicant for KEMBLE LIQUID HANDLING SYSTEM DISPENSER?

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

What is the FDA product code for KEMBLE LIQUID HANDLING SYSTEM DISPENSER?

The FDA product code for KEMBLE LIQUID HANDLING SYSTEM DISPENSER is JQW.

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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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