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Aggro/Link Control Software

by Chrono-Log Corp

510(k) K932566

Aggro/Link Control Software is a Class II device made by Chrono-Log Corp, cleared under FDA 510(k) K932566 on 2 Nov 1993, active as of 11 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 11 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 11 Oct 2026.

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK932566 Date2 Nov 1993ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JBX
FDA applicant
Chrono-Log Corp.
Device class
Class II
Regulation
21 CFR Part 864.6675
Advisory committee
Hematology
FDA decision
SESE Substantially Equivalent

Devices cleared under K932566

3 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K932566
UDI-DISize and differences
CHRONO-LOG AGGRO/LINK Opti8 Software
CHRONO-LOG CORP
AGGRO/LINK Opti8 Software00811476011663 —On the market
CHRONO-LOG AGGRO/LINK WBA Software
CHRONO-LOG CORP
AGGRO/LINK WBA Software00811476011007 —On the market
CHRONO-LOG AGGRO/LINK8 Software
CHRONO-LOG CORP
AGGRO/LINK8 Software00811476011021 —On the market

Similar devices

Other devices filed under FDA product code JBX (Aggregrometer, Platelet).

Other devices from Chrono-Log Corp

See all devices from Chrono-Log Corp →