Lactose

FDA 510(k) K833210 · Acumedia Manufacturers, Inc.

Substantially Equivalent

510(k) numberK833210

Submission

Device name
Lactose
Applicant
Acumedia Manufacturers, Inc.
Mchenry, IL, US
Received
September 19, 1983
Decision date
October 27, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSK – Supplement, Culture Media
Device class
Class I (low risk)
Regulation
21 CFR 866.2450
Specialty
Microbiology

Other 510(k)s with product code JSK

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K881949Ats Nac-Pac SetJSK · Traditional Alpha-Tec Systems, Inc.05/25/1988SE
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K881566Hemoglobin PowderJSK · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K861997Penicillin-Streptomycin-Fungizone MixtureJSK · Traditional Hazleton Research Products, Inc.06/10/1986SE
K861824Gentamicin Sulfate Solution (10MG Gentamicin)JSK · Traditional Flow Laboratories, Inc.05/20/1986SE
K861823Gentamicin Sulfate Solution (50MG Gentamicin)JSK · Traditional Flow Laboratories, Inc.05/20/1986SE
K861791Penicillin-Streptomycin-FungizoneJSK · Traditional Flow Laboratories, Inc.05/20/1986SE
K855172Kwi (TM) G-Co/TwoJSK · Traditional Micro-Bio-Logics02/20/1986SE
K853546Abbott Cation Supplement SolutionJSK · Traditional Abbott Laboratories09/06/1985SE
K850302Suplex & Suplex DiluentJSK · Traditional Pro-Lab, Inc.03/22/1985SE

More from Pro-Lab, 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 Lactose cleared by the FDA?

Lactose (K833210) received a 510(k) decision of Substantially Equivalent on October 27, 1983, 38 days after the submission was received.

What is the product code of K833210?

The FDA product code is JSK – Supplement, Culture Media, a Class I (low risk) device regulated under 21 CFR 866.2450.