Chemmate(Tm) Lambda

FDA 510(k) K950149 · Biotek Solutions, Inc.

Substantially Equivalent

510(k) numberK950149

Submission

Device name
Chemmate(Tm) Lambda
Applicant
Biotek Solutions, Inc.
Santa Barbara, CA, US
Received
January 17, 1995
Decision date
December 6, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DEH – Lambda, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5550
Specialty
Immunology

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More from The Binding Site, Ltd.

510(k)DeviceDecision
K950148Chemmate(Tm) CD43DEH · Traditional 07/02/1996SE
K936111Chemmate Special Stain LCA-CD45DEH · Traditional 02/27/1996SE
K950152Chemmate(Tm) UCHL1 (CD45-RO)DFH · Traditional 10/27/1995SE
K950150Chemmate(Tm) KappaDFH · Traditional 10/27/1995SE
K950151Chemmate(Tm) L26 (CD20)DEH · Traditional 10/04/1995SE

Questions and answers

When was Chemmate(Tm) Lambda cleared by the FDA?

Chemmate(Tm) Lambda (K950149) received a 510(k) decision of Substantially Equivalent on December 6, 1995, 323 days after the submission was received.

What is the product code of K950149?

The FDA product code is DEH – Lambda, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5550.