FDA 510(k)

SELENITE BROTH

K-Number: K881576 · 1988-04-18

Decision Date1988-04-18

Product CodeJSI

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SELENITE BROTH 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 K881576. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELENITE BROTH?

SELENITE BROTH 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 K881576.

When did SELENITE BROTH receive FDA 510(k) clearance?

SELENITE BROTH received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881576.

Who is the listed applicant for SELENITE BROTH?

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 SELENITE BROTH?

The FDA product code for SELENITE BROTH is JSI.

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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: JSI)

K070691BBL CHROMAGAR 0157Becton, Dickinson & CO K974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia 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.