Aves Wright Stain

FDA 510(k) K820437 · Helena Laboratories

Substantially Equivalent

510(k) numberK820437

Submission

Device name
Aves Wright Stain
Applicant
Helena Laboratories
Mchenry, IL, US
Received
February 17, 1982
Decision date
March 26, 1982
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
K890674Accustain(Tm) - Automated Wright Giemsa Stain SetIAF · Traditional Sigma Diagnostics, Inc.02/24/1989SE
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

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Questions and answers

When was Aves Wright Stain cleared by the FDA?

Aves Wright Stain (K820437) received a 510(k) decision of Substantially Equivalent on March 26, 1982, 37 days after the submission was received.

What is the product code of K820437?

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