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FDA 510(k)

ECLIPSE

K-Number: K821007 · 1982-05-03

ApplicantScientific Software & Instrument Co.
Decision Date1982-05-03
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ECLIPSE is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Software & Instrument Co.. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K821007. 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 ECLIPSE?

ECLIPSE is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Scientific Software & Instrument Co.. The 510(k) number is K821007.

When did ECLIPSE receive FDA 510(k) clearance?

ECLIPSE received FDA 510(k) clearance on 1982-05-03, under 510(k) number K821007.

Who is the listed applicant for ECLIPSE?

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

What is the FDA product code for ECLIPSE?

The FDA product code for ECLIPSE 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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