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FDA 510(k)

ENOXACIN 10 MCG. SENSI SISC

K-Number: K923952 · 1992-09-18

ApplicantBecton Dickinson Microbiology Systems
Decision Date1992-09-18
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ENOXACIN 10 MCG. SENSI SISC is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Microbiology Systems. It received FDA 510(k) clearance on 1992-09-18 under 510(k) number K923952. 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 ENOXACIN 10 MCG. SENSI SISC?

ENOXACIN 10 MCG. SENSI SISC is a medical device that received FDA 510(k) clearance on 1992-09-18. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K923952.

When did ENOXACIN 10 MCG. SENSI SISC receive FDA 510(k) clearance?

ENOXACIN 10 MCG. SENSI SISC received FDA 510(k) clearance on 1992-09-18, under 510(k) number K923952.

Who is the listed applicant for ENOXACIN 10 MCG. SENSI SISC?

The FDA 510(k) record lists Becton Dickinson Microbiology Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENOXACIN 10 MCG. SENSI SISC?

The FDA product code for ENOXACIN 10 MCG. SENSI SISC is JTN.

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Other records listing Becton Dickinson Microbiology Systems 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.

K993577CEFOTAXIME/CLAVULANIC, 30/10UG, BBL SENSI-DISC AND CEFTAZIDIME/CLAVULANIC ACID, 30/10UG, BBL SENSI-DISCK984631BDPROBETEC ET CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE AMPLIFIED DNA ASSAYK981517CEFDINIR, 5 UG, SENSI-DISCK980683TROVAFLOXACIN 10G, SENSI-DISCK974578GREPAFLOXACIN, 5 MG, SENSI-DISCK970333BACTEC MYCO/F LYTIC CULTURE VIALS

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Related Devices (Code: JTN)

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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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