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FDA 510(k)

LOWENSTEIN-JENSEN, SELECTIVE

K-Number: K880125 · 1988-03-31

ApplicantHardy Media
Decision Date1988-03-31
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LOWENSTEIN-JENSEN, SELECTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880125. 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 LOWENSTEIN-JENSEN, SELECTIVE?

LOWENSTEIN-JENSEN, SELECTIVE is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Hardy Media. The 510(k) number is K880125.

When did LOWENSTEIN-JENSEN, SELECTIVE receive FDA 510(k) clearance?

LOWENSTEIN-JENSEN, SELECTIVE received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880125.

Who is the listed applicant for LOWENSTEIN-JENSEN, SELECTIVE?

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 LOWENSTEIN-JENSEN, SELECTIVE?

The FDA product code for LOWENSTEIN-JENSEN, SELECTIVE 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.

K880126LAURYL TRYPTOSE BROTHK880134MIDDLEBROOK 7H11 AGARK880133MIL MEDIUMK880131LOWENSTEIN-JENSEN, GRUFTK880122MIDDLEBROOK 7H9 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.K881572XL AGAR BASEAcumedia 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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