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FDA 510(k)

SDI PREPAX DILUKIT CA

K-Number: K840042 · 1984-02-10

ApplicantScientific Distributors, Inc.
Decision Date1984-02-10
Product Code
DecisionSubstantially Equivalent

Device Summary

SDI PREPAX DILUKIT CA 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 1984-02-10 under 510(k) number K840042. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SDI PREPAX DILUKIT CA?

SDI PREPAX DILUKIT CA is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Scientific Distributors, Inc.. The 510(k) number is K840042.

When did SDI PREPAX DILUKIT CA receive FDA 510(k) clearance?

SDI PREPAX DILUKIT CA received FDA 510(k) clearance on 1984-02-10, under 510(k) number K840042.

Who is the listed applicant for SDI PREPAX DILUKIT CA?

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

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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.K840044SDI PREPAX DILUKIT 29-1000K840041SDI PREPAX DILUKIT HWK840043SDI PREPAX DILUKIT CTK840038PREPAX DILUKIT PLUS

View all 7 devices →

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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