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FDA 510(k)

IAFP X.L.D. AGAR

K-Number: K872669 · 1987-08-11

ApplicantI.A.F. Production, Inc.
Decision Date1987-08-11
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IAFP X.L.D. AGAR is the device name listed in this FDA 510(k) record. The listed applicant is I.A.F. Production, Inc.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K872669. 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 IAFP X.L.D. AGAR?

IAFP X.L.D. AGAR is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872669.

When did IAFP X.L.D. AGAR receive FDA 510(k) clearance?

IAFP X.L.D. AGAR received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872669.

Who is the listed applicant for IAFP X.L.D. AGAR?

The FDA 510(k) record lists I.A.F. Production, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IAFP X.L.D. AGAR?

The FDA product code for IAFP X.L.D. AGAR is JSI.

Other records listing I.A.F. Production, 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.

K872690IAFP V. AGAR SELECTIVEK872681IAFP C.D.C. ANAEROBIC AGAR W/5% SHEEP BLOODK872672IAFP BILE ESCULIN AZIDE AGARK872683IAFP BILE ESCULIN AGARK872689IAFP SABOURAUD DEXTROSE AGARK872691IAFP UREA AGAR SLANT

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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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