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FDA 510(k)

NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

K-Number: K984036 · 1999-01-13

ApplicantOxoid , Ltd.
Decision Date1999-01-13
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid , Ltd.. It received FDA 510(k) clearance on 1999-01-13 under 510(k) number K984036. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC?

NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC is a medical device that received FDA 510(k) clearance on 1999-01-13. The listed applicant is Oxoid , Ltd.. The 510(k) number is K984036.

When did NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC receive FDA 510(k) clearance?

NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC received FDA 510(k) clearance on 1999-01-13, under 510(k) number K984036.

Who is the listed applicant for NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC?

The FDA 510(k) record lists Oxoid , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC?

The FDA product code for NETILMICIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC is JTN.

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Other records listing Oxoid , Ltd. as applicant

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K070262ERTAPENEM ANTIMICROBIAL SUSCEPTIBILITY TEST DISCK060286TIGECYCLINE ANTIMICROBIAL SUSCEPTIBILITY TEST DISCK042157DAPTOMYCIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISCK011710OXOID PBP2 1 LATEX AGGLUTINATION TESTK012588OXOID PYLORI TEST KIT, MODEL DR0130MK010536MOXIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

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Related Devices (Code: JTN)

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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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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