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FDA 510(k)

G C II AGAR WITH SENSIVITALEX

K-Number: K932879 · 1993-09-21

ApplicantBecton Dickinson Microbiology Systems
Decision Date1993-09-21
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

G C II AGAR WITH SENSIVITALEX 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 1993-09-21 under 510(k) number K932879. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G C II AGAR WITH SENSIVITALEX?

G C II AGAR WITH SENSIVITALEX is a medical device that received FDA 510(k) clearance on 1993-09-21. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K932879.

When did G C II AGAR WITH SENSIVITALEX receive FDA 510(k) clearance?

G C II AGAR WITH SENSIVITALEX received FDA 510(k) clearance on 1993-09-21, under 510(k) number K932879.

Who is the listed applicant for G C II AGAR WITH SENSIVITALEX?

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 G C II AGAR WITH SENSIVITALEX?

The FDA product code for G C II AGAR WITH SENSIVITALEX is JSO.

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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: JSO)

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.

K190553HardyCHROM CREHardy DiagnosticsK181092CHROMID CARBA agar (CARB)Biomerieux S.A.K171061MRSASelect IIBio-RadK162620Remel Spectra ESBLRemel, Inc.K160512HardyCHROM ESBLHardy DiagnosticsK162076chromID MRSAbioMerieux, 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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