IL TEST (TM) PT-FIBRINOGEN HS PLUS

FDA 510(k) Premarket Notification · Submission K933252 · Applicant: Instrumentation Laboratory CO

Public Record 510(k) Submission Decision Date: 1993-10-04 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K933252.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K933252
Applicant / Sponsor
Device Name
IL TEST (TM) PT-FIBRINOGEN HS PLUS
Product Code
GJS
Decision Date
1993-10-04
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Hematology (HE)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1993-07-02

Related Establishments / Registrations

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