Accurun 121 Hav Igm Positive Control

FDA 510(k) K971657 · Boston Biomedica, Inc.

Substantially Equivalent

510(k) numberK971657

Submission

Device name
Accurun 121 Hav Igm Positive Control
Applicant
Boston Biomedica, Inc.
West Bridgewater, MA, US
Received
May 6, 1997
Decision date
August 12, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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More from Aalto Scientific, Ltd.

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K974261Accurun 135 Toxoplasma Igg Positive ControlLJK · Traditional 12/11/1997SE
K972986Accurun 140 Rubella Igg Positive ControlMJX · Traditional 10/08/1997SE
K972884Accurun 146 CMV Igm Positive ControlLKQ · Traditional 08/22/1997SE
K972048Accurun 117 Hbeag Positive ControlJJY · Traditional 08/12/1997SE
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Questions and answers

When was Accurun 121 Hav Igm Positive Control cleared by the FDA?

Accurun 121 Hav Igm Positive Control (K971657) received a 510(k) decision of Substantially Equivalent on August 12, 1997, 98 days after the submission was received.

What is the product code of K971657?

The FDA product code is JJY – Multi-Analyte Controls, All Kinds (Assayed), a Class I (low risk) device regulated under 21 CFR 862.1660.