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FDA 510(k)

HISTO-CHECK LEGIONELLA CONTROL SLIDES

K-Number: K883567 · 1988-10-06

ApplicantVal Tech Diagnostics, Inc.
Decision Date1988-10-06
Product CodeLJG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HISTO-CHECK LEGIONELLA 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 1988-10-06 under 510(k) number K883567. The device is classified under product code LJG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTO-CHECK LEGIONELLA CONTROL SLIDES?

HISTO-CHECK LEGIONELLA CONTROL SLIDES is a medical device that received FDA 510(k) clearance on 1988-10-06. The listed applicant is Val Tech Diagnostics, Inc.. The 510(k) number is K883567.

When did HISTO-CHECK LEGIONELLA CONTROL SLIDES receive FDA 510(k) clearance?

HISTO-CHECK LEGIONELLA CONTROL SLIDES received FDA 510(k) clearance on 1988-10-06, under 510(k) number K883567.

Who is the listed applicant for HISTO-CHECK LEGIONELLA 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 HISTO-CHECK LEGIONELLA CONTROL SLIDES?

The FDA product code for HISTO-CHECK LEGIONELLA CONTROL SLIDES is LJG.

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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.

K883568HISTO-CHECK ACID FAST SLIDESK883569HISTO-CHECK GRAM NEGATIVE SLIDESK883570HISTO-CHECK FUNGAL CONTROL SLIDESK883571HISTO-CHECK PARASITIC CONTROL SLIDESK883684HERPES VIRUS CONTROL SLIDESK883232HISTONE REACTIVE ANA

View all 11 devices →

Related Devices (Code: LJG)

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.

K943228MICROSPORIDIUM CONTROL SETMeridian Diagnostics, Inc.K924893MICROSPORIDIUM CONTROL SLIDEScientific Device Laboratory, Inc.K890670CRYPTOSPORIDIUM CONTROL SLIDEScientific Device Laboratory, Inc.K890718GRAM STAIN CONTROL SLIDEScientific Device Laboratory, Inc.K890616BION DIRECT IDENTIFICATION CONTROL SLIDEBion Ent., Ltd.K883569HISTO-CHECK GRAM NEGATIVE SLIDESVal Tech Diagnostics, 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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