FDA 510(k)

OF BASAL MEDIUM

K-Number: K881550 · 1988-04-18

Decision Date1988-04-18

Product CodeJSG

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

OF BASAL MEDIUM 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 1988-04-18 under 510(k) number K881550. 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 OF BASAL MEDIUM?

OF BASAL MEDIUM is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K881550.

When did OF BASAL MEDIUM receive FDA 510(k) clearance?

OF BASAL MEDIUM received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881550.

Who is the listed applicant for OF BASAL MEDIUM?

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 OF BASAL MEDIUM?

The FDA product code for OF BASAL MEDIUM 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.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia Manufacturers, Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881554SKIM MILK DEHYDRATEDAcumedia 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.