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FDA 510(k)

BRUCELLA AGAR MODIFIED

K-Number: K833299 · 1983-11-07

ApplicantAcumedia Manufacturers, Inc.
Decision Date1983-11-07
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BRUCELLA AGAR MODIFIED 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 1983-11-07 under 510(k) number K833299. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUCELLA AGAR MODIFIED?

BRUCELLA AGAR MODIFIED is a medical device that received FDA 510(k) clearance on 1983-11-07. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833299.

When did BRUCELLA AGAR MODIFIED receive FDA 510(k) clearance?

BRUCELLA AGAR MODIFIED received FDA 510(k) clearance on 1983-11-07, under 510(k) number K833299.

Who is the listed applicant for BRUCELLA AGAR MODIFIED?

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 BRUCELLA AGAR MODIFIED?

The FDA product code for BRUCELLA AGAR MODIFIED is JSG.

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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.

K881575SELECTIVE STREPTOCOCCUS AGARK881540FLO AGARK881544LITTMAN AGARK881561TERGITOL 7 BROTHK881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGARK881569STUARTS TRANSPORT MEDIUM

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Related Devices (Code: JSG)

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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 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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