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FDA 510(k)

GC II AGAR WITH ISOVITALEX

K-Number: K932882 · 1993-09-24

Decision Date1993-09-24
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GC II AGAR WITH ISOVITALEX 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 1993-09-24 under 510(k) number K932882. 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 GC II AGAR WITH ISOVITALEX?

GC II AGAR WITH ISOVITALEX is a medical device that received FDA 510(k) clearance on 1993-09-24. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K932882.

When did GC II AGAR WITH ISOVITALEX receive FDA 510(k) clearance?

GC II AGAR WITH ISOVITALEX received FDA 510(k) clearance on 1993-09-24, under 510(k) number K932882.

Who is the listed applicant for GC II AGAR WITH ISOVITALEX?

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 GC II AGAR WITH ISOVITALEX?

The FDA product code for GC II AGAR WITH ISOVITALEX is JSO.

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.

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.

View all 33 devices →

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.

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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