Spia Sys for Solid Phase Immunoassays

FDA 510(k) K831448 · R&D Systems, Inc.

Substantially Equivalent

510(k) numberK831448

Submission

Device name
Spia Sys for Solid Phase Immunoassays
Applicant
R&D Systems, Inc.
Mchenry, IL, US
Received
May 5, 1983
Decision date
June 8, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LIB – Device, General Purpose, Microbiology, Diagnostic
Device class
Class I (low risk)
Regulation
21 CFR 866.2660
Specialty
Microbiology

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Questions and answers

When was Spia Sys for Solid Phase Immunoassays cleared by the FDA?

Spia Sys for Solid Phase Immunoassays (K831448) received a 510(k) decision of Substantially Equivalent on June 8, 1983, 34 days after the submission was received.

What is the product code of K831448?

The FDA product code is LIB – Device, General Purpose, Microbiology, Diagnostic, a Class I (low risk) device regulated under 21 CFR 866.2660.