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FDA 510(k)

DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT

K-Number: K931922 · 1994-03-30

ApplicantViratest Intl., Inc.
Decision Date1994-03-30
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT is the device name listed in this FDA 510(k) record. The listed applicant is Viratest Intl., Inc.. It received FDA 510(k) clearance on 1994-03-30 under 510(k) number K931922. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT?

DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Viratest Intl., Inc.. The 510(k) number is K931922.

When did DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT receive FDA 510(k) clearance?

DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT received FDA 510(k) clearance on 1994-03-30, under 510(k) number K931922.

Who is the listed applicant for DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT?

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

What is the FDA product code for DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT?

The FDA product code for DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT is JSM.

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Other records listing Viratest Intl., 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.

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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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