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FDA 510(k)

SHIGELLA I.D.

K-Number: K821337 · 1982-05-28

ApplicantAnalytical Products, Inc.
Decision Date1982-05-28
Product CodeGNB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SHIGELLA I.D. is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K821337. The device is classified under product code GNB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIGELLA I.D.?

SHIGELLA I.D. is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Analytical Products, Inc.. The 510(k) number is K821337.

When did SHIGELLA I.D. receive FDA 510(k) clearance?

SHIGELLA I.D. received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821337.

Who is the listed applicant for SHIGELLA I.D.?

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

What is the FDA product code for SHIGELLA I.D.?

The FDA product code for SHIGELLA I.D. is GNB.

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Related Devices (Code: GNB)

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.

K961537SAS SHIGELLA SONNEI FORM II ANTISERUMSa Scientific, Inc.K961549SAS SHIGELLA FLEXNERI TYPE 2 ANTISERUMSa Scientific, Inc.K961535SAS SHIGELLA DYSENTERIAE GROUP A1 (8-10) ANTISERUMSa Scientific, Inc.K961534SAS SHIGELLA SONNEI FORM I ANTISERUM (3/100/1000ML)Sa Scientific, Inc.K961553SAS SHIGELLA DYSENTERIAE TYPE 1 ANTISERUMSa Scientific, Inc.K961540SAS SHIGELLA SONNEI GROUP D ANTISERUMSa Scientific, 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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