SIGMA DIAGNOSTICS ACCUCLOT CONTROL I— 510(k) K981248

Substantially Equivalent

Sigma Diagnostics, Inc.

FDA 510(k) clearance K981248 for SIGMA DIAGNOSTICS ACCUCLOT CONTROL I, Substantially Equivalent on 1998-04-29. Applicant: Sigma Diagnostics, Inc..

Clearance details

Applicant
Sigma Diagnostics, Inc.
Product code
Code GGN
Advisory panel
Hematology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Louis, MO, US
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