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FDA 510(k)

ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN

K-Number: K872698 · 1987-09-18

ApplicantSita, Inc.
Decision Date1987-09-18
Product CodeGOA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN is the device name listed in this FDA 510(k) record. The listed applicant is Sita, Inc.. It received FDA 510(k) clearance on 1987-09-18 under 510(k) number K872698. The device is classified under product code GOA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN?

ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN is a medical device that received FDA 510(k) clearance on 1987-09-18. The listed applicant is Sita, Inc.. The 510(k) number is K872698.

When did ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN receive FDA 510(k) clearance?

ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN received FDA 510(k) clearance on 1987-09-18, under 510(k) number K872698.

Who is the listed applicant for ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN?

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

What is the FDA product code for ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN?

The FDA product code for ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN is GOA.

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 Sita, 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.

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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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