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FDA 510(k)

CANNU-SKREEN-PRELIMINARY

K-Number: K841831 · 1984-07-06

ApplicantBiochemical Diagnostic, Inc.
Decision Date1984-07-06
Product CodeDKE
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CANNU-SKREEN-PRELIMINARY is the device name listed in this FDA 510(k) record. The listed applicant is Biochemical Diagnostic, Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K841831. The device is classified under product code DKE. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNU-SKREEN-PRELIMINARY?

CANNU-SKREEN-PRELIMINARY is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Biochemical Diagnostic, Inc.. The 510(k) number is K841831.

When did CANNU-SKREEN-PRELIMINARY receive FDA 510(k) clearance?

CANNU-SKREEN-PRELIMINARY received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841831.

Who is the listed applicant for CANNU-SKREEN-PRELIMINARY?

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

What is the FDA product code for CANNU-SKREEN-PRELIMINARY?

The FDA product code for CANNU-SKREEN-PRELIMINARY is DKE.

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Other records listing Biochemical Diagnostic, Inc. as applicant

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K121122DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROLK050328PREGNANCY-SKREENK925586DETECTABUSE(TM)K904181ANTI-GBM ANTIBODIES QUANTITATIVE KIT

Related Devices (Code: DKE)

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.

K003687VERDICT II THC/COC/OPI/AMP, VERDICTII THC/COC/OPI,VERDICT II THC/COC/AMP,VERDICT II THC/COC/PCP,VERDICT II THC/COCMedtox Diagnostics, Inc.K994405INSTANT-VIEW MARIJUANA URINE CASSETTE TESTAlfa Scientific Designs, Inc.K992068STATUS STIK, ACCUSIGN STIKPrinceton BioMeditech Corp.K991751STATUS CUP ACCUSIGN CUPPrinceton BioMeditech Corp.K991078ACCUSIGN DOA8, DOA8 PANEL, THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA8, THC/OPI/COC/AMP/BZO/BAR/TCA/PAP, STATUS DS DO8Princeton BioMeditech Corp.K983147ACCUSIGN DOA 8, ACCUSIGN DOA 8 PANEL, ACCUSIGN THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA 8, BIOSIGN THC/OPI/COC/AMP/PPrinceton BioMeditech Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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