Tryptic Soy Agar W/5% Sheep Blood & Emb

FDA 510(k) K811474 · Biomedia, Inc.

Substantially Equivalent

510(k) numberK811474

Submission

Device name
Tryptic Soy Agar W/5% Sheep Blood & Emb
Applicant
Biomedia, Inc.
Mchenry, IL, US
Received
May 26, 1981
Decision date
June 18, 1981
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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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
K821300#2010 Camphylobacter AgarJSI · Traditional 06/02/1982SE
K821302#50003 Quad Diagnostic SystemJSH · Traditional 06/01/1982SE
K821301#50002 Quad Diagnostic SystemJSI · Traditional 06/01/1982SE
K821108Bi Plate-Xld/Hektoen #30012JSI · Traditional 05/13/1982SE
K811479Chodolate Agar, EnrichedJTY · Traditional 06/18/1981SE
K811478Emb Agar, LevineJSI · Traditional 06/18/1981SE
K811477Macconkey AgarJSI · Traditional 06/18/1981SE
K811476Thayer Martin AgarJTY · Traditional 06/18/1981SE
K811475Tryptic Soy Agar W/5% & 10% Sheep BloodJSG · Traditional 06/18/1981SE
K811473Mueller Hinton Agar W/5% Sheep BloodJTZ · Traditional 06/18/1981SE

Questions and answers

When was Tryptic Soy Agar W/5% Sheep Blood & Emb cleared by the FDA?

Tryptic Soy Agar W/5% Sheep Blood & Emb (K811474) received a 510(k) decision of Substantially Equivalent on June 18, 1981, 23 days after the submission was received.

What is the product code of K811474?

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