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FDA 510(k)

SDI PREPAX DILUKIT 29-1000

K-Number: K840044 · 1984-03-09

ApplicantScientific Distributors, Inc.
Decision Date1984-03-09
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SDI PREPAX DILUKIT 29-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Distributors, Inc.. It received FDA 510(k) clearance on 1984-03-09 under 510(k) number K840044. The device is classified under product code JJO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SDI PREPAX DILUKIT 29-1000?

SDI PREPAX DILUKIT 29-1000 is a medical device that received FDA 510(k) clearance on 1984-03-09. The listed applicant is Scientific Distributors, Inc.. The 510(k) number is K840044.

When did SDI PREPAX DILUKIT 29-1000 receive FDA 510(k) clearance?

SDI PREPAX DILUKIT 29-1000 received FDA 510(k) clearance on 1984-03-09, under 510(k) number K840044.

Who is the listed applicant for SDI PREPAX DILUKIT 29-1000?

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

What is the FDA product code for SDI PREPAX DILUKIT 29-1000?

The FDA product code for SDI PREPAX DILUKIT 29-1000 is JJO.

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Other records listing Scientific Distributors, 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.

K892658SDI PREPAX COUNTAPETTE KITK851320SDI PREPAX DILUKIT M.K840041SDI PREPAX DILUKIT HWK840043SDI PREPAX DILUKIT CTK840038PREPAX DILUKIT PLUSK840042SDI PREPAX DILUKIT CA

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Related Devices (Code: JJO)

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K873603FINNIGAN MAT INCOS 50Finnigan Corp.K862148OLYMPUS AU 5000 FLAME PHOTOMETER MODULEOlympus Corp.K843375ELVI 655 FLAME PHOTOMETERLogos Scientific, Inc.K841847LITHIUM REAGENTReagent Laboratory, Inc.K834226FLAME PHOTOMETERSDr. Bruno Lange GmbHK841422VOLUME TEST DYE 6Reagent Laboratory, Inc.

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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