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FDA 510(k)

WELLWASH 4 MARK II

K-Number: K922803 · 1992-11-05

ApplicantDenley Instruments, Inc.
Decision Date1992-11-05
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WELLWASH 4 MARK II is the device name listed in this FDA 510(k) record. The listed applicant is Denley Instruments, Inc.. It received FDA 510(k) clearance on 1992-11-05 under 510(k) number K922803. 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 WELLWASH 4 MARK II?

WELLWASH 4 MARK II is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Denley Instruments, Inc.. The 510(k) number is K922803.

When did WELLWASH 4 MARK II receive FDA 510(k) clearance?

WELLWASH 4 MARK II received FDA 510(k) clearance on 1992-11-05, under 510(k) number K922803.

Who is the listed applicant for WELLWASH 4 MARK II?

The FDA 510(k) record lists Denley Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WELLWASH 4 MARK II?

The FDA product code for WELLWASH 4 MARK II is JQW.

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Other records listing Denley Instruments, Inc. 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.

K922327DENLEY WELLPREP 2 SAMPLE PROCESSORK922183WELLPREP 2000 SAMPLE PROCESSORK915284STACKING MICROPLATE WASHERK913567WELLPREP 1K900599MICROPLATE REAGENT DISPENSERK894270DENLEY ANTHOS 2001 READER

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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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