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FDA 510(k)

SYSTEM WASHER 100

K-Number: K936258 · 1994-04-26

ApplicantEg&G Berthold
Decision Date1994-04-26
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYSTEM WASHER 100 is the device name listed in this FDA 510(k) record. The listed applicant is Eg&G Berthold. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K936258. 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 SYSTEM WASHER 100?

SYSTEM WASHER 100 is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Eg&G Berthold. The 510(k) number is K936258.

When did SYSTEM WASHER 100 receive FDA 510(k) clearance?

SYSTEM WASHER 100 received FDA 510(k) clearance on 1994-04-26, under 510(k) number K936258.

Who is the listed applicant for SYSTEM WASHER 100?

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

What is the FDA product code for SYSTEM WASHER 100?

The FDA product code for SYSTEM WASHER 100 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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