FDA 510(k)

BCYE AGAR

K-Number: K880140 · 1988-03-30

Decision Date1988-03-30

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

BCYE 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 1988-03-30 under 510(k) number K880140. 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 BCYE AGAR?

BCYE AGAR 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 K880140.

When did BCYE AGAR receive FDA 510(k) clearance?

BCYE AGAR received FDA 510(k) clearance on 1988-03-30, under 510(k) number K880140.

Who is the listed applicant for BCYE 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 BCYE AGAR?

The FDA product code for BCYE AGAR is JSJ.

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 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.