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FDA 510(k)

YEAST BEEF AGAR-ANTIBIOTIC MED.4

K-Number: K833218 · 1983-10-27

ApplicantAcumedia Manufacturers, Inc.
Decision Date1983-10-27
Product CodeLKA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YEAST BEEF AGAR-ANTIBIOTIC MED.4 is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K833218. 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 YEAST BEEF AGAR-ANTIBIOTIC MED.4?

YEAST BEEF AGAR-ANTIBIOTIC MED.4 is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833218.

When did YEAST BEEF AGAR-ANTIBIOTIC MED.4 receive FDA 510(k) clearance?

YEAST BEEF AGAR-ANTIBIOTIC MED.4 received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833218.

Who is the listed applicant for YEAST BEEF AGAR-ANTIBIOTIC MED.4?

The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YEAST BEEF AGAR-ANTIBIOTIC MED.4?

The FDA product code for YEAST BEEF AGAR-ANTIBIOTIC MED.4 is LKA.

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Other records listing Acumedia Manufacturers, 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.

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGARK881540FLO AGARK881544LITTMAN AGARK881561TERGITOL 7 BROTHK881575SELECTIVE STREPTOCOCCUS AGARK881569STUARTS TRANSPORT MEDIUM

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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.K872688IAFP MUELLER HINTON AGAR W/5% SHEEP BLOODI.A.F. Production, Inc.K833207AK AGAR 2Acumedia 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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