Xylose Lysine Deoxycholate Agar

FDA 510(k) K821605 · Hardy Media

Substantially Equivalent

510(k) numberK821605

Submission

Device name
Xylose Lysine Deoxycholate Agar
Applicant
Hardy Media
Mchenry, IL, US
Received
May 28, 1982
Decision date
July 6, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSI – Culture Media, Selective And Differential
Device class
Class I (low risk)
Regulation
21 CFR 866.2360
Specialty
Microbiology

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K891593Listeria Selective Enrichment MediumJSI · Traditional Oxoid U.S.A., Inc.06/09/1989SE
K890199Dentocult Sm-Strip MutansJSI · Traditional Orion Corp.03/02/1989SE
K882182Salmonella-Shigella (SS) Agar - Product #P3326JSI · Traditional Lakewood Biochemical Co., Inc.06/06/1988SE
K881577Modified Selective Streptococcus AgarJSI · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881576Selenite BrothJSI · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881575Selective Streptococcus AgarJSI · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881572XL Agar BaseJSI · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881556Trichomonas BrothJSI · Traditional Acumedia Manufacturers, Inc.04/18/1988SE

More from Acumedia Manufacturers, Inc.

510(k)DeviceDecision
K880134Middlebrook 7H11 AgarKZI · Traditional 03/31/1988SE
K880133Mil MediumJSE · Traditional 03/31/1988SE
K880131Lowenstein-Jensen, GruftKZI · Traditional 03/31/1988SE
K880126Lauryl Tryptose BrothJSF · Traditional 03/31/1988SE
K880125Lowenstein-Jensen, SelectiveJSI · Traditional 03/31/1988SE
K880124Lowenstein-Jensen, W/NaclJSJ · Traditional 03/31/1988SE
K880123Lowenstein-Jensen SlantJSJ · Traditional 03/31/1988SE
K880122Middlebrook 7H9 BrothKZI · Traditional 03/31/1988SE
K880121Moellers Decarboxylase, BaseJSH · Traditional 03/31/1988SE
K880120Moellers Decarboxylase, LysineJSF · Traditional 03/31/1988SE

Questions and answers

When was Xylose Lysine Deoxycholate Agar cleared by the FDA?

Xylose Lysine Deoxycholate Agar (K821605) received a 510(k) decision of Substantially Equivalent on July 6, 1982, 39 days after the submission was received.

What is the product code of K821605?

The FDA product code is JSI – Culture Media, Selective And Differential, a Class I (low risk) device regulated under 21 CFR 866.2360.