Cystine Tryptic Medium

FDA 510(k) K834007 · Micro Media Laboratories

Substantially Equivalent

510(k) numberK834007

Submission

Device name
Cystine Tryptic Medium
Applicant
Micro Media Laboratories
Mchenry, IL, US
Received
November 21, 1983
Decision date
December 22, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSQ – Chromatography For Bacterial Identification
Device class
Class I (low risk)
Regulation
21 CFR 862.2250
Specialty
Clinical Chemistry

Other 510(k)s with product code JSQ

510(k)DeviceApplicantDecision
K811138Nutrient AgarJSQ · Traditional Acumedia Manufacturers, Inc.05/05/1981SE
K761226GP3%SP-2100DOHON100/120 Mesh SupelcoportJSQ · Traditional Supelco, Inc.01/14/1977SE

More from Supelco, Inc.

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K853691Tergitol 7 AgarJSI · Traditional 09/17/1985SE
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K851348Coba AgarJSJ · Traditional 04/19/1985SE
K851347Kanamycin-Vancomycin-Laked Blood AgarJSJ · Traditional 04/19/1985SE
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K851345Purple BrothJSH · Traditional 04/19/1985SE
K851343Brom Cresol Purple StarchJSH · Traditional 04/19/1985SE
K850848Brain Heart Infusion AgarJSG · Traditional 03/20/1985SE
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Questions and answers

When was Cystine Tryptic Medium cleared by the FDA?

Cystine Tryptic Medium (K834007) received a 510(k) decision of Substantially Equivalent on December 22, 1983, 31 days after the submission was received.

What is the product code of K834007?

The FDA product code is JSQ – Chromatography For Bacterial Identification, a Class I (low risk) device regulated under 21 CFR 862.2250.