Accustain(Tm) - Automated Wright Giemsa Stain Set

FDA 510(k) K890674 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK890674

Submission

Device name
Accustain(Tm) - Automated Wright Giemsa Stain Set
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
February 9, 1989
Decision date
February 24, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IAF – Wright'S Stain
Device class
Class I (low risk)
Regulation
21 CFR 864.1850
Specialty
Hematology

Other 510(k)s with product code IAF

510(k)DeviceApplicantDecision
K890673Wright-Glemsa StainIAF · Traditional Sigma Diagnostics, Inc.02/24/1989SE
K854236Histamine Ria Test for Histamine Biological FluidsIAF · Traditional Nms Pharmaceuticals, Inc.10/10/1986SN
K860793Camco Stain PakIAF · Traditional Cambridge Chemical Products, Inc.03/18/1986SE
K853241Hematology Stain PackIAF · Traditional Fisher Scientific Co., LLC08/19/1985SE
K852138Wescor Stain Pack for Model 7100 Aerospray Slide SIAF · Traditional Canyon Diagnostics, Inc.06/13/1985SE
K842744Wright StainIAF · Traditional E K Ind., Inc.08/12/1984SE
K842745Wright-Giemsa Quick StainIAF · Traditional E K Ind., Inc.08/10/1984SE
K833678Hematology Wright's Stain PackIAF · Traditional J.S. Medical Assoc.11/25/1983SE
K833260Stain Pack for Aerospray Slide StainerIAF · Traditional Wescor, Inc.10/28/1983SE
K831605Hematology PakIAF · Traditional Mercedes Scientific Co., Inc.06/30/1983SE

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Questions and answers

When was Accustain(Tm) - Automated Wright Giemsa Stain Set cleared by the FDA?

Accustain(Tm) - Automated Wright Giemsa Stain Set (K890674) received a 510(k) decision of Substantially Equivalent on February 24, 1989, 15 days after the submission was received.

What is the product code of K890674?

The FDA product code is IAF – Wright'S Stain, a Class I (low risk) device regulated under 21 CFR 864.1850.