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FDA 510(k)

MICRO ORGANISM GROWTH SYS-M1000

K-Number: K843000 · 1985-02-06

ApplicantHml Inc/Biotechnology Transfer
Decision Date1985-02-06
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICRO ORGANISM GROWTH SYS-M1000 is the device name listed in this FDA 510(k) record. The listed applicant is Hml Inc/Biotechnology Transfer. It received FDA 510(k) clearance on 1985-02-06 under 510(k) number K843000. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO ORGANISM GROWTH SYS-M1000?

MICRO ORGANISM GROWTH SYS-M1000 is a medical device that received FDA 510(k) clearance on 1985-02-06. The listed applicant is Hml Inc/Biotechnology Transfer. The 510(k) number is K843000.

When did MICRO ORGANISM GROWTH SYS-M1000 receive FDA 510(k) clearance?

MICRO ORGANISM GROWTH SYS-M1000 received FDA 510(k) clearance on 1985-02-06, under 510(k) number K843000.

Who is the listed applicant for MICRO ORGANISM GROWTH SYS-M1000?

The FDA 510(k) record lists Hml Inc/Biotechnology Transfer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO ORGANISM GROWTH SYS-M1000?

The FDA product code for MICRO ORGANISM GROWTH SYS-M1000 is LIO.

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 Hml Inc/Biotechnology Transfer 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.

K842310HEMATOLOGY ANALYZERK842311CHEMISTRY ANALYZER, GEN. PURPOSE

Related Devices (Code: LIO)

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.

K222613ARX Liquid Amies Collection & Transport SystemArx Sciences, Inc.K131630PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEMPuritan Medical Products, LLCK120846TRANSPORT CULTURE MEDIUM DEVICEPuritan Medical Products, LLCK103805MEDICAL WIRE & EQUIPMENT S-TRANSWAB (OR SIGMA-TRANSWAB) LIQUID AMIES COLLECTION AND TRANSPORT DEVICEMedical Wire & Equipment Company (Bath), Ltd.K082472VIROCULT, MODEL MW950Medical Wire & Equipment Company (Bath), Ltd.K070062COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USEDiesse Diagnostica Senese S.P.A.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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