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FDA 510(k)

ATS MEDIA

K-Number: K880130 · 1988-03-30

ApplicantHardy Media
Decision Date1988-03-30
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ATS MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1988-03-30 under 510(k) number K880130. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATS MEDIA?

ATS MEDIA is a medical device that received FDA 510(k) clearance on 1988-03-30. The listed applicant is Hardy Media. The 510(k) number is K880130.

When did ATS MEDIA receive FDA 510(k) clearance?

ATS MEDIA received FDA 510(k) clearance on 1988-03-30, under 510(k) number K880130.

Who is the listed applicant for ATS MEDIA?

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

What is the FDA product code for ATS MEDIA?

The FDA product code for ATS MEDIA is JSI.

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Other records listing Hardy Media 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.

K880134MIDDLEBROOK 7H11 AGARK880122MIDDLEBROOK 7H9 BROTHK880131LOWENSTEIN-JENSEN, GRUFTK880133MIL MEDIUMK880126LAURYL TRYPTOSE BROTHK880116MRVP BROTH

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Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia Manufacturers, 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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