Immunoglobulins G

FDA 510(k) K873870 · Unipath , Ltd.

Substantially Equivalent

510(k) numberK873870

Submission

Device name
Immunoglobulins G
Applicant
Unipath , Ltd.
Bedford Mk41 Oqg, GB
Received
August 24, 1987
Decision date
October 13, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DEW – Igg, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5510
Specialty
Immunology

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Questions and answers

When was Immunoglobulins G cleared by the FDA?

Immunoglobulins G (K873870) received a 510(k) decision of Substantially Equivalent on October 13, 1987, 50 days after the submission was received.

What is the product code of K873870?

The FDA product code is DEW – Igg, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5510.