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FDA 510(k)

SXT BLOOD AGAR

K-Number: K832860 · 1983-09-26

ApplicantTroy Biologicals, Inc.
Decision Date1983-09-26
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SXT BLOOD AGAR 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 1983-09-26 under 510(k) number K832860. 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 SXT BLOOD AGAR?

SXT BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K832860.

When did SXT BLOOD AGAR receive FDA 510(k) clearance?

SXT BLOOD AGAR received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832860.

Who is the listed applicant for SXT BLOOD AGAR?

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 SXT BLOOD AGAR?

The FDA product code for SXT BLOOD AGAR 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-5000K832863STREP ID QUADK832862TRANSGROW MEDIUMK832861SABOURAUD DEXTROSE AGARK823307CAMPYLOBACTER SELECTIVE AGARK823311COLUMBIA V AGAR W/5% HUMAN BLOOD

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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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