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FDA 510(k)

IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD

K-Number: K872666 · 1987-08-07

ApplicantI.A.F. Production, Inc.
Decision Date1987-08-07
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD 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 1987-08-07 under 510(k) number K872666. 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 IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD?

IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872666.

When did IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD receive FDA 510(k) clearance?

IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD received FDA 510(k) clearance on 1987-08-07, under 510(k) number K872666.

Who is the listed applicant for IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD?

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 K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD?

The FDA product code for IAFP K.V. ANAEROBIC AGAR W/5% SHEEP BLOOD is JSJ.

Related Clinical Trials

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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: 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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