FDA 510(k) Premarket Notification K852537: T-3 RIASSAY

Submission Details & Decision

Normalized public record details for 510(k) notification K852537.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K852537

Applicant / Sponsor

Ria Diagnostics

Device Name

T-3 RIASSAY

Product Code

CDP

Decision Date

1985-08-12

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Clinical Chemistry (CH)

Clearance Type

Traditional

Third Party Flag

Date Received

1985-06-14

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