Septi-Chek Columbia Broth Blood Culture

FDA 510(k) K812730 · Hoffmann-La Roche, Inc.

Substantially Equivalent

510(k) numberK812730

Submission

Device name
Septi-Chek Columbia Broth Blood Culture
Applicant
Hoffmann-La Roche, Inc.
Mchenry, IL, US
Received
September 28, 1981
Decision date
October 23, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSG – Culture Media, Non-Selective And Non-Differential
Device class
Class I (low risk)
Regulation
21 CFR 866.2300
Specialty
Microbiology

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K882495Thioglycollate Broth W/Vita. K & Hemin - #T3007JSG · Traditional Lakewood Biochemical Co., Inc.07/01/1988SE
K881564Tryptose Blood Agar Base W/Yeast ExtractJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881563Tryptose Phosphate BrothJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881562Tryptose Blood Agar BaseJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881558Tryptose AgarJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881557TryptoneJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881554Skim Milk DehydratedJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881550Of Basal MediumJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881548MPH AgarJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881546Malt Extract AgarJSG · Traditional Acumedia Manufacturers, Inc.04/18/1988SE

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Questions and answers

When was Septi-Chek Columbia Broth Blood Culture cleared by the FDA?

Septi-Chek Columbia Broth Blood Culture (K812730) received a 510(k) decision of Substantially Equivalent on October 23, 1981, 25 days after the submission was received.

What is the product code of K812730?

The FDA product code is JSG – Culture Media, Non-Selective And Non-Differential, a Class I (low risk) device regulated under 21 CFR 866.2300.