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FDA 510(k)

DFA RESPIRATORY VIRUS SCREENING & ID KIT

K-Number: K022713 · 2002-12-18

ApplicantDiagnostic Hybrids, Inc.
Decision Date2002-12-18
Product CodeGNW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DFA RESPIRATORY VIRUS SCREENING & ID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Hybrids, Inc.. It received FDA 510(k) clearance on 2002-12-18 under 510(k) number K022713. The device is classified under product code GNW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DFA RESPIRATORY VIRUS SCREENING & ID KIT?

DFA RESPIRATORY VIRUS SCREENING & ID KIT is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Diagnostic Hybrids, Inc.. The 510(k) number is K022713.

When did DFA RESPIRATORY VIRUS SCREENING & ID KIT receive FDA 510(k) clearance?

DFA RESPIRATORY VIRUS SCREENING & ID KIT received FDA 510(k) clearance on 2002-12-18, under 510(k) number K022713.

Who is the listed applicant for DFA RESPIRATORY VIRUS SCREENING & ID KIT?

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

What is the FDA product code for DFA RESPIRATORY VIRUS SCREENING & ID KIT?

The FDA product code for DFA RESPIRATORY VIRUS SCREENING & ID KIT is GNW.

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Other records listing Diagnostic Hybrids, 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.

K092229THYRETAIN TM TSI REPORTER BIOASSAYK093415D3 FASTPOINT L-DFA PARAINFLUENZA VIRUS/ADENOVIRUS IDENTIFICATION KITK093233D3 FASTPOINT L-DFA RSV/MVP IDENTIFICATION KITK092882D3 FASTPOINT L-DFA INFLUENZA A/INFLUENZA B VIRUS IDENTIFICATION KITK091171D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KITK091753ELVIS HSV ID AND D3 TYPING TEST SYSTEM

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Related Devices (Code: GNW)

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.

K092882D3 FASTPOINT L-DFA INFLUENZA A/INFLUENZA B VIRUS IDENTIFICATION KITDiagnostic Hybrids, Inc.K092300MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KITDiagnostic Hybrids, Inc.K081746D3 DUET DFA INFLUENZA A/RESPIRATORY VIRUS SCREENING KITDiagnostic Hybrids, Inc.K061101D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KITDiagnostic Hybrids, Inc.K003204BARTELS VIRAL RESPIRATORY SCREENING AND IDENTIFICATION KITIntracel Corp.K974302LIGHT DIAGNOSTICS SIMULFLUOR FLU A/FLU BLight 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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