Cobas Integra Reagent Cassettes for Albumin, Hbalc and Digoxin

FDA 510(k) K961824 · Roche Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK961824

Submission

Device name
Cobas Integra Reagent Cassettes for Albumin, Hbalc and Digoxin
Applicant
Roche Diagnostic Systems, Inc.
Somerville, NJ, US
Received
May 10, 1996
Decision date
July 23, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DCF – Albumin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5040
Specialty
Immunology

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Questions and answers

When was Cobas Integra Reagent Cassettes for Albumin, Hbalc and Digoxin cleared by the FDA?

Cobas Integra Reagent Cassettes for Albumin, Hbalc and Digoxin (K961824) received a 510(k) decision of Substantially Equivalent on July 23, 1996, 74 days after the submission was received.

What is the product code of K961824?

The FDA product code is DCF – Albumin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5040.