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FDA 510(k)

DERMATOPHYTE TEST MEDIUM

K-Number: K834010 · 1984-01-03

ApplicantMicro Media Laboratories
Decision Date1984-01-03
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DERMATOPHYTE TEST MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K834010. 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 DERMATOPHYTE TEST MEDIUM?

DERMATOPHYTE TEST MEDIUM is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Micro Media Laboratories. The 510(k) number is K834010.

When did DERMATOPHYTE TEST MEDIUM receive FDA 510(k) clearance?

DERMATOPHYTE TEST MEDIUM received FDA 510(k) clearance on 1984-01-03, under 510(k) number K834010.

Who is the listed applicant for DERMATOPHYTE TEST MEDIUM?

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

What is the FDA product code for DERMATOPHYTE TEST MEDIUM?

The FDA product code for DERMATOPHYTE TEST MEDIUM is JSJ.

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Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851343BROM CRESOL PURPLE STARCHK851348COBA AGAR

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Related Devices (Code: JSJ)

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.

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.

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