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FDA 510(k)

GAS GENERATING KIT SYSTEM FOR CAMPYLOB.

K-Number: K802494 · 1980-11-12

Decision Date1980-11-12
Product CodeKZJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GAS GENERATING KIT SYSTEM FOR CAMPYLOB. is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802494. The device is classified under product code KZJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS GENERATING KIT SYSTEM FOR CAMPYLOB.?

GAS GENERATING KIT SYSTEM FOR CAMPYLOB. is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K802494.

When did GAS GENERATING KIT SYSTEM FOR CAMPYLOB. receive FDA 510(k) clearance?

GAS GENERATING KIT SYSTEM FOR CAMPYLOB. received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802494.

Who is the listed applicant for GAS GENERATING KIT SYSTEM FOR CAMPYLOB.?

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

What is the FDA product code for GAS GENERATING KIT SYSTEM FOR CAMPYLOB.?

The FDA product code for GAS GENERATING KIT SYSTEM FOR CAMPYLOB. is KZJ.

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 Oxoid U.S.A., Inc. 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 93 devices →

Related Devices (Code: KZJ)

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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