Biotis Ld-Presumpto Quadrant Plate

FDA 510(k) K842424 · Otisville Biotech, Inc.

Substantially Equivalent

510(k) numberK842424

Submission

Device name
Biotis Ld-Presumpto Quadrant Plate
Applicant
Otisville Biotech, Inc.
Mchenry, IL, US
Received
June 20, 1984
Decision date
July 2, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSE – Culture Media, Multiple Biochemical Test
Device class
Class I (low risk)
Regulation
21 CFR 866.2320
Specialty
Microbiology

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K883995X-Act Urea/TdaJSE · Traditional Pro-Lab, Inc.10/12/1988SE
K880133Mil MediumJSE · Traditional Hardy Media03/31/1988SE
K880116MRVP BrothJSE · Traditional Hardy Media03/31/1988SE
K874537Kligler Iron Agar and Triple Sugar Iron AgarJSE · Traditional Lakewood Biochemical Co., Inc.11/20/1987SE
K871096Cystine Tryptic Agar W/O CarbohydratesJSE · Traditional bioMerieux, Inc.04/03/1987SE
K864674Microdilution Identification PanelsJSE · Traditional American Micro Scan01/05/1987SE
K862393Biotis Litmus MilkJSE · Traditional Otisville Biotech, Inc.07/03/1986SE
K860415Biotis Simmon Citrate AgarJSE · Traditional Otisville Biotech, Inc.02/24/1986SE

More from Otisville Biotech, Inc.

510(k)DeviceDecision
K862400Biotis KV Laked Blood AgarJSJ · Traditional 07/03/1986SE
K862399Biotis SXT AgarJSJ · Traditional 07/03/1986SE
K862398Biotis Decarboxylase Media, OrnithineJSF · Traditional 07/03/1986SE
K862397Biotis Decarboxylase Media, LysineJSF · Traditional 07/03/1986SE
K862396Biotis Decarboxylase Media, ArginineJSF · Traditional 07/03/1986SE
K862395Biotis Decarboxylase Media, BaseJSH · Traditional 07/03/1986SE
K862394Biotis Mitis SalivariusJSI · Traditional 07/03/1986SE
K862393Biotis Litmus MilkJSE · Traditional 07/03/1986SE
K862392Biotis Motility Test MediumJSF · Traditional 07/03/1986SE
K862391Biotis Desoxycholate AgarJSI · Traditional 07/03/1986SE

Questions and answers

When was Biotis Ld-Presumpto Quadrant Plate cleared by the FDA?

Biotis Ld-Presumpto Quadrant Plate (K842424) received a 510(k) decision of Substantially Equivalent on July 2, 1984, 12 days after the submission was received.

What is the product code of K842424?

The FDA product code is JSE – Culture Media, Multiple Biochemical Test, a Class I (low risk) device regulated under 21 CFR 866.2320.