FDA 510(k)

ACIDICASE-BB1

K-Number: K833209 · 1983-10-27

Decision Date1983-10-27

Product CodeJSG

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ACIDICASE-BB1 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 K833209. 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 ACIDICASE-BB1?

ACIDICASE-BB1 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 K833209.

When did ACIDICASE-BB1 receive FDA 510(k) clearance?

ACIDICASE-BB1 received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833209.

Who is the listed applicant for ACIDICASE-BB1?

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 ACIDICASE-BB1?

The FDA product code for ACIDICASE-BB1 is JSG.

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Other records listing Acumedia Manufacturers, Inc. as applicant

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGAR K881540FLO AGAR K881544LITTMAN AGAR K881561TERGITOL 7 BROTH K881575SELECTIVE STREPTOCOCCUS AGAR K881569STUARTS TRANSPORT MEDIUM

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Related Devices (Code: JSG)

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.