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FDA 510(k)

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS

K-Number: K861022 · 1986-04-04

ApplicantMicro-Bio-Logics
Decision Date1986-04-04
Product CodeJTR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Bio-Logics. It received FDA 510(k) clearance on 1986-04-04 under 510(k) number K861022. The device is classified under product code JTR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS?

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Micro-Bio-Logics. The 510(k) number is K861022.

When did KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS receive FDA 510(k) clearance?

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS received FDA 510(k) clearance on 1986-04-04, under 510(k) number K861022.

Who is the listed applicant for KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS?

The FDA 510(k) record lists Micro-Bio-Logics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS?

The FDA product code for KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS is JTR.

Related Clinical Trials

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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Other records listing Micro-Bio-Logics 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.

K870731LYFO KWIK(TM) RUS KITK861312LYFO-KWIK (TM) COAGULASE PLASMAK855172KWI (TM) G-CO/TWOK855198INDI KWIK (TM) CO/TWO KITK852998NEISSERIA - KWIK PLUSK851978LYFO-KWIK OMI KIT

View all 9 devices →

Related Devices (Code: JTR)

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.

K871121PROTECT T.M.Pro-Lab, Inc.K862914FEKAL CHECK PARASITOLOGY CONTROL SLIDETrend Scientific, Inc.K855198INDI KWIK (TM) CO/TWO KITMicro-Bio-LogicsK842579B.E.C. GROWTH CHEK MICROBIAL SUSPENSIONSBiological & Environmental Control LaboratoriesK842129LYFO-DISK MICROORGANISMSMicro-Bio-LogicsK831653LYOPHILIZED MICROORGANISMSAustin Biological Laboratories

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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