Ebv-Na Test

FDA 510(k) K880043 · Gull Laboratories, Inc.

Substantially Equivalent

510(k) numberK880043

Submission

Device name
Ebv-Na Test
Applicant
Gull Laboratories, Inc.
Salt Lake City, UT, US
Received
January 6, 1988
Decision date
March 24, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LLM – Test, Antigen, Nuclear, Epstein-Barr Virus
Device class
Class I (low risk)
Regulation
21 CFR 866.3235
Specialty
Microbiology

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More from Incstar Corp.

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K962343Toxo Igg Elisa TestLGD · Traditional 03/24/1997SE
K935730Ebna Igg Elisa TestLLM · Traditional 09/19/1995SE
K940093Ebv-Ea(D) Igg Elisa TestLSE · Traditional 09/15/1995SE
K941046VZV Igg Elisa TestLFY · Traditional 08/24/1995SE
K941198Ebv LGG Elisa TestLSE · Traditional 08/23/1995SE
K932333Protectoral Ultrasonic Handpiece ProcessorEFB · Traditional 08/15/1995SE
K941624Rubella Igg Elisa TestLFX · Traditional 08/04/1995SE
K922759HSV-2 Igm Elisa Test--ModificationLGC · Traditional 10/05/1992SE

Questions and answers

When was Ebv-Na Test cleared by the FDA?

Ebv-Na Test (K880043) received a 510(k) decision of Substantially Equivalent on March 24, 1988, 78 days after the submission was received.

What is the product code of K880043?

The FDA product code is LLM – Test, Antigen, Nuclear, Epstein-Barr Virus, a Class I (low risk) device regulated under 21 CFR 866.3235.