Amnio Stat-Flm Agglutination Test

FDA 510(k) K834616 · Hana Biologics, Inc.

Substantially Equivalent

510(k) numberK834616

Submission

Device name
Amnio Stat-Flm Agglutination Test
Applicant
Hana Biologics, Inc.
Walker, MI, US
Received
December 14, 1983
Decision date
May 25, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHG – Chromatographic Separation, Lecithin/Sphingomyelin Ratio
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1455
Specialty
Clinical Chemistry

Other 510(k)s with product code JHG

510(k)DeviceApplicantDecision
K061549Amniostat-Flm-PgJHG · Traditional Irvine Scientific Sales Co., Inc.10/18/2006SE
K871593TDXR Fetal Lung MaturityJHG · Traditional Abbott Laboratories07/20/1987SE
K822150Amnistat-FlmJHG · Traditional Hana Biologics, Inc.10/21/1982SE
K813216Secure Fdi Test KitJHG · Traditional Beckman Instruments, Inc.12/17/1981SE
K811588Helena Fetal-Tek 200 MethodJHG · Traditional Helena Laboratories06/25/1981SE
K790798Fetal Maturity Test ProcedureJHG · Traditional Helena Laboratories06/05/1979SE

More from Helena Laboratories

510(k)DeviceDecision
K883682Chang Medium (Additional Indications)KIT · Traditional 09/16/1988SE
K855205Mycotrim TM VL Triphasic Culture SystemJSI · Traditional 02/05/1986SE
K833933Ace Color TestKQN · Traditional 03/23/1984SE
K822737Mycotrium-RsJSI · Traditional 12/03/1982SE
K822736Mycotrium-GuJSI · Traditional 12/03/1982SE
K822150Amnistat-FlmJHG · Traditional 10/21/1982SE
K812820Chang MediumKIT · Traditional 11/10/1981SE

Questions and answers

When was Amnio Stat-Flm Agglutination Test cleared by the FDA?

Amnio Stat-Flm Agglutination Test (K834616) received a 510(k) decision of Substantially Equivalent on May 25, 1984, 163 days after the submission was received.

What is the product code of K834616?

The FDA product code is JHG – Chromatographic Separation, Lecithin/Sphingomyelin Ratio, a Class II (moderate risk) device regulated under 21 CFR 862.1455.