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Sigma Diagnostics Auto D-Dimer Calibrator, Model A7971

by Sigma Diagnostics, Inc. 510(k)

Active United States

510(k) K013549

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK013549 Date26 Dec 2001ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 10 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
DAP
Device Class
Class II
Regulation
21 CFR Part 864.7320
Advisory Committee
Hematology
FDA Decision
SESE Substantially Equivalent

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