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FDA 510(k)

HERPES VIRUS CONTROL SLIDES

K-Number: K883684 · 1988-09-28

ApplicantVal Tech Diagnostics, Inc.
Decision Date1988-09-28
Product CodeGQN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HERPES VIRUS CONTROL SLIDES is the device name listed in this FDA 510(k) record. The listed applicant is Val Tech Diagnostics, Inc.. It received FDA 510(k) clearance on 1988-09-28 under 510(k) number K883684. The device is classified under product code GQN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERPES VIRUS CONTROL SLIDES?

HERPES VIRUS CONTROL SLIDES is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is Val Tech Diagnostics, Inc.. The 510(k) number is K883684.

When did HERPES VIRUS CONTROL SLIDES receive FDA 510(k) clearance?

HERPES VIRUS CONTROL SLIDES received FDA 510(k) clearance on 1988-09-28, under 510(k) number K883684.

Who is the listed applicant for HERPES VIRUS CONTROL SLIDES?

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

What is the FDA product code for HERPES VIRUS CONTROL SLIDES?

The FDA product code for HERPES VIRUS CONTROL SLIDES is GQN.

Related Clinical Trials

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Other records listing Val Tech Diagnostics, 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.

K883571HISTO-CHECK PARASITIC CONTROL SLIDESK883568HISTO-CHECK ACID FAST SLIDESK883569HISTO-CHECK GRAM NEGATIVE SLIDESK883570HISTO-CHECK FUNGAL CONTROL SLIDESK883567HISTO-CHECK LEGIONELLA CONTROL SLIDESK883232HISTONE REACTIVE ANA

View all 11 devices →

Related Devices (Code: GQN)

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.

K070265DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION AND TYPING KIT, MODEL 01-090000Diagnostic Hybrids, Inc.K063798DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION KIT, MODEL 01-080000Diagnostic Hybrids, Inc.K991880LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAYLight DiagnosticsK971662ELVIS HSV ID/TYPING TEST SYSTEMDiagnostic Hybrids, Inc.K971101HSV-2 ANTIGEN CONTROL SLIDESViral Antigens, Inc.K964874HSV-1 ANTIGEN CONTROL SLIDESViral Antigens, 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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