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FDA 510(k)

LYFO KWIK(TM) RUS KIT

K-Number: K870731 · 1987-06-17

ApplicantMicro-Bio-Logics
Decision Date1987-06-17
Product CodeJXA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LYFO KWIK(TM) RUS KIT 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 1987-06-17 under 510(k) number K870731. The device is classified under product code JXA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYFO KWIK(TM) RUS KIT?

LYFO KWIK(TM) RUS KIT is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is Micro-Bio-Logics. The 510(k) number is K870731.

When did LYFO KWIK(TM) RUS KIT receive FDA 510(k) clearance?

LYFO KWIK(TM) RUS KIT received FDA 510(k) clearance on 1987-06-17, under 510(k) number K870731.

Who is the listed applicant for LYFO KWIK(TM) RUS KIT?

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 LYFO KWIK(TM) RUS KIT?

The FDA product code for LYFO KWIK(TM) RUS KIT is JXA.

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.

K861312LYFO-KWIK (TM) COAGULASE PLASMAK861022KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMSK855172KWI (TM) G-CO/TWOK855198INDI KWIK (TM) CO/TWO KITK852998NEISSERIA - KWIK PLUSK851978LYFO-KWIK OMI KIT

View all 9 devices →

Related Devices (Code: JXA)

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.

K011043OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OMA-UTI)OsmetechK981084URISCREENDiatech Diagnostics,Inc.K972676URINE SCREENING DEVICECombact Diagnostic Systems , Ltd.K952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KITTri-Tech, Inc.K950257MULTIPLE (IZON DBS & URINE COLLECTION KIT)Izon Business Products, Inc.K950246MULTIPLE (IZON URINE COLLECTION KIT)Izon Business Products, 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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