Feeley-Gorman Agar

FDA 510(k) K833301 · Acumedia Manufacturers, Inc.

Substantially Equivalent

510(k) numberK833301

Submission

Device name
Feeley-Gorman Agar
Applicant
Acumedia Manufacturers, Inc.
Mchenry, IL, US
Received
September 22, 1983
Decision date
October 28, 1983
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
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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
K881579Amies Transport Medium W/O CharcoalJSN · Traditional 04/18/1988SE
K881578StreptoselJSJ · Traditional 04/18/1988SE
K881577Modified Selective Streptococcus AgarJSI · Traditional 04/18/1988SE
K881576Selenite BrothJSI · Traditional 04/18/1988SE
K881575Selective Streptococcus AgarJSI · Traditional 04/18/1988SE
K881574W-L Differential MediumJSJ · Traditional 04/18/1988SE
K881573Phytone Yeast Extract AgarJSJ · Traditional 04/18/1988SE
K881572XL Agar BaseJSI · Traditional 04/18/1988SE
K881571Ym BrothJSJ · Traditional 04/18/1988SE
K881570Sabouraud Maltose AgarJSJ · Traditional 04/18/1988SE

Questions and answers

When was Feeley-Gorman Agar cleared by the FDA?

Feeley-Gorman Agar (K833301) received a 510(k) decision of Substantially Equivalent on October 28, 1983, 36 days after the submission was received.

What is the product code of K833301?

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