Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD

K-Number: K872688 · 1987-08-11

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

Device Summary

IAFP MUELLER HINTON 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 1987-08-11 under 510(k) number K872688. The device is classified under product code LKA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD?

IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD 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 K872688.

When did IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD receive FDA 510(k) clearance?

IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872688.

Who is the listed applicant for IAFP MUELLER HINTON 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 MUELLER HINTON AGAR W/5% SHEEP BLOOD?

The FDA product code for IAFP MUELLER HINTON AGAR W/5% SHEEP BLOOD is LKA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 29 devices →

Related Devices (Code: LKA)

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.

K872687IAFP MUELLER HINTON AGAR W/HEMO. W/CVA ENRICHMENTI.A.F. Production, Inc.K872686IAFP MUELLER HINTON AGARI.A.F. Production, Inc.K833207AK AGAR 2Acumedia Manufacturers, Inc.K833218YEAST BEEF AGAR-ANTIBIOTIC MED.4Acumedia 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.

↑