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FDA 510(k)

DERMOTOPHYTE TEST MEDIUM

K-Number: K810181 · 1981-02-05

ApplicantTroy Biologicals, Inc.
Decision Date1981-02-05
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DERMOTOPHYTE TEST MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Troy Biologicals, Inc.. It received FDA 510(k) clearance on 1981-02-05 under 510(k) number K810181. 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 DERMOTOPHYTE TEST MEDIUM?

DERMOTOPHYTE TEST MEDIUM is a medical device that received FDA 510(k) clearance on 1981-02-05. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K810181.

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

DERMOTOPHYTE TEST MEDIUM received FDA 510(k) clearance on 1981-02-05, under 510(k) number K810181.

Who is the listed applicant for DERMOTOPHYTE TEST MEDIUM?

The FDA 510(k) record lists Troy Biologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMOTOPHYTE TEST MEDIUM?

The FDA product code for DERMOTOPHYTE TEST MEDIUM is JSJ.

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Other records listing Troy Biologicals, Inc. 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.

K861301BACTI PLATE (DERMATOLOGY) PRODUCT NO. PS-5000K832860SXT BLOOD AGARK832861SABOURAUD DEXTROSE AGARK832862TRANSGROW MEDIUMK832863STREP ID QUADK823310STREPTOCOCCUS SELECTIVE 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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