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Technicon Autogrouper 16-C System

by Technicon Instruments Corp. 510(k)

Active United States

510(k) K810899

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK810899 Date5 May 1981ClearedStatusActive

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  • Withdrawn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 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KSZ
Device Class
Class II
Regulation
21 CFR Part 864.9175
Advisory Committee
Hematology
FDA Decision
SESE Substantially Equivalent

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