Amerlite Reproductive Endocrinology (Label Change)

FDA 510(k) K890708 · Amersham Corp.

Substantially Equivalent

510(k) numberK890708

Submission

Device name
Amerlite Reproductive Endocrinology (Label Change)
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
January 31, 1989
Decision date
March 20, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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More from Aalto Scientific, Ltd.

510(k)DeviceDecision
K914135Amerlite(Tm) PROLACTIN-30 Assay, LAN.0086/2086CFT · Traditional 02/18/1992SE
K912733Amerlex-M Specific Estrol(Unconjugated) Ria KitCIG · Traditional 07/22/1991SE
K912766Amerlite Ck-Mb AssayJHY · Traditional 07/17/1991SE
K904666Amerlite TSH-60 Assay Product Code: Lan. 0008/2008JLW · Traditional 11/02/1990SE
K902760Amersham TSH Control SeraJJX · Traditional 07/27/1990SE
K901857GADOLINIUM-153 Bone Densitometer (GDC.10413)KGI · Traditional 07/09/1990SE
K901854GADOLINIUM-153 Bone Densitometer (GDC.10411/10412)KGI · Traditional 07/09/1990SE
K901848GADOLINIUM-153 Bone Densitometer SourcesKGI · Traditional 07/09/1990SE
K901832GADOLINIUM-153 Bone Densitometer Sources GDC.10415KGI · Traditional 07/09/1990SE
K896270Amerlite ESTRADIOL-60 Assay LAN.0081/2081CHP · Traditional 12/12/1989SE

Questions and answers

When was Amerlite Reproductive Endocrinology (Label Change) cleared by the FDA?

Amerlite Reproductive Endocrinology (Label Change) (K890708) received a 510(k) decision of Substantially Equivalent on March 20, 1989, 48 days after the submission was received.

What is the product code of K890708?

The FDA product code is JJY – Multi-Analyte Controls, All Kinds (Assayed), a Class I (low risk) device regulated under 21 CFR 862.1660.