Api 20C

FDA 510(k) K771008 · Analytical Products, Inc.

Substantially Equivalent

510(k) numberK771008

Submission

Device name
Api 20C
Applicant
Analytical Products, Inc.
Mchenry, IL, US
Received
June 3, 1977
Decision date
August 3, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JXB – Kit, Identification, Yeast
Device class
Class I (low risk)
Regulation
21 CFR 866.2660
Specialty
Microbiology

Other 510(k)s with product code JXB

510(k)DeviceApplicantDecision
K080719Yeast Traffic Light Pna FishJXB · Traditional Advandx, Inc.09/12/2008SE
K062461C. Albicans Pna FishJXB · Traditional Advandx, Inc.10/25/2006SE
K993554YeastestJXB · Traditional Diagnostic Markers, Inc.02/10/2000SE
K943621Rapid Yeast Plus SystemJXB · Traditional Innovative Diagnostic Systems, Inc.01/27/1995SE
K935124Bacticard CandidaJXB · Traditional Remel Co.02/25/1994SE
K900112Microring YtJXB · Traditional Medical Wire & Equipment Co.07/31/1990SE
K881925Vitek Yeast Biochemical CardJXB · Traditional Vitek Systems, Inc.06/16/1988SE
K860575Yeast Identification PanelJXB · Traditional American Micro Scan05/13/1986SE
K830286Yeast IdentJXB · Traditional Analytical Products, Inc.04/05/1983SE
K802309MS-2 Identification SystemJXB · Traditional Abbott Laboratories12/01/1980SE

More from Abbott Laboratories

510(k)DeviceDecision
K924814Api 20E/UNISCEPT 20EJSS · Traditional 03/11/1993SE
K923684Api Uniscept Mic/Type 2 and 3 and Micro MicJWY · Traditional 12/03/1992SE
K922926Api Uniscept Kb/Type 2 and 3JWY · Traditional 10/13/1992SE
K901559Modification to Api Uniscept 20GPLQL · Traditional 09/10/1990SE
K901390Dmac Indole ReagentJTO · Traditional 04/16/1990SE
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

Questions and answers

When was Api 20C cleared by the FDA?

Api 20C (K771008) received a 510(k) decision of Substantially Equivalent on August 3, 1977, 61 days after the submission was received.

What is the product code of K771008?

The FDA product code is JXB – Kit, Identification, Yeast, a Class I (low risk) device regulated under 21 CFR 866.2660.