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FDA 510(k)

HEMOPHILUS QUAD 10 PLATE

K-Number: K823306 · 1982-12-15

ApplicantTroy Biologicals, Inc.
Decision Date1982-12-15
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HEMOPHILUS QUAD 10 PLATE 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 1982-12-15 under 510(k) number K823306. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOPHILUS QUAD 10 PLATE?

HEMOPHILUS QUAD 10 PLATE is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K823306.

When did HEMOPHILUS QUAD 10 PLATE receive FDA 510(k) clearance?

HEMOPHILUS QUAD 10 PLATE received FDA 510(k) clearance on 1982-12-15, under 510(k) number K823306.

Who is the listed applicant for HEMOPHILUS QUAD 10 PLATE?

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 HEMOPHILUS QUAD 10 PLATE?

The FDA product code for HEMOPHILUS QUAD 10 PLATE is JSI.

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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 AGARK832863STREP ID QUADK832861SABOURAUD DEXTROSE AGARK832862TRANSGROW MEDIUMK823311COLUMBIA V AGAR W/5% HUMAN BLOOD

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Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia 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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