Dmac Indole Reagent

FDA 510(k) K901390 · Analytical Products, Inc.

Substantially Equivalent

510(k) numberK901390

Submission

Device name
Dmac Indole Reagent
Applicant
Analytical Products, Inc.
Plainview, NY, US
Received
March 26, 1990
Decision date
April 16, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JTO – Discs, Strips And Reagents, Microorganism Differentiation
Device class
Class I (low risk)
Regulation
21 CFR 866.2660
Specialty
Microbiology

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K901559Modification to Api Uniscept 20GPLQL · Traditional 09/10/1990SE
K895796Api Uniscept KBJWY · Traditional 11/13/1989SE
K884510Modification Micro-MicJWY · Traditional 11/22/1988SE
K884509Modification Mic/Api Uniscept(R)JWY · Traditional 11/22/1988SE
K880598Modifications to Api Uniscept (R) KBJWY · Traditional 03/23/1988SE
K874466Api Uniscept(R) Micro-Mic(R) System/Uniscept MicJWY · Traditional 12/09/1987SE
K865062Aladin (TM)LRG · Traditional 03/25/1987SE

Questions and answers

When was Dmac Indole Reagent cleared by the FDA?

Dmac Indole Reagent (K901390) received a 510(k) decision of Substantially Equivalent on April 16, 1990, 21 days after the submission was received.

What is the product code of K901390?

The FDA product code is JTO – Discs, Strips And Reagents, Microorganism Differentiation, a Class I (low risk) device regulated under 21 CFR 866.2660.