Api 3S

FDA 510(k) K770176 · Analytical Products, Inc.

Substantially Equivalent

510(k) numberK770176

Submission

Device name
Api 3S
Applicant
Analytical Products, Inc.
Mchenry, IL, US
Received
January 26, 1977
Decision date
February 18, 1977
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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K874537Kligler Iron Agar and Triple Sugar Iron AgarJSE · Traditional Lakewood Biochemical Co., Inc.11/20/1987SE
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K864674Microdilution Identification PanelsJSE · Traditional American Micro Scan01/05/1987SE
K862393Biotis Litmus MilkJSE · Traditional Otisville Biotech, Inc.07/03/1986SE
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More from Otisville Biotech, Inc.

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 3S cleared by the FDA?

Api 3S (K770176) received a 510(k) decision of Substantially Equivalent on February 18, 1977, 23 days after the submission was received.

What is the product code of K770176?

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