FDA 510(k)

MIDDLEBROOK 7H11 SELECTIVE AGAR

K-Number: K870645 · 1987-04-14

Decision Date1987-04-14

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

MIDDLEBROOK 7H11 SELECTIVE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1987-04-14 under 510(k) number K870645. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDDLEBROOK 7H11 SELECTIVE AGAR?

MIDDLEBROOK 7H11 SELECTIVE AGAR is a medical device that received FDA 510(k) clearance on 1987-04-14. The listed applicant is Hardy Media. The 510(k) number is K870645.

When did MIDDLEBROOK 7H11 SELECTIVE AGAR receive FDA 510(k) clearance?

MIDDLEBROOK 7H11 SELECTIVE AGAR received FDA 510(k) clearance on 1987-04-14, under 510(k) number K870645.

Who is the listed applicant for MIDDLEBROOK 7H11 SELECTIVE AGAR?

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 MIDDLEBROOK 7H11 SELECTIVE AGAR?

The FDA product code for MIDDLEBROOK 7H11 SELECTIVE AGAR is JSJ.

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Other records listing Hardy Media as applicant

K880134MIDDLEBROOK 7H11 AGAR K880122MIDDLEBROOK 7H9 BROTH K880131LOWENSTEIN-JENSEN, GRUFT K880133MIL MEDIUM K880126LAURYL TRYPTOSE BROTH K880116MRVP BROTH

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Related Devices (Code: JSJ)

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia Manufacturers, Inc.

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.