ACL 6000 SYSTEM (ACL 6000)— 510(k) K961991

Substantially Equivalent

Instrumentation Laboratory CO

FDA 510(k) clearance K961991 for ACL 6000 SYSTEM (ACL 6000), Substantially Equivalent on 1996-09-04. Applicant: Instrumentation Laboratory CO. Device class: 2.

Clearance details

Applicant
Instrumentation Laboratory CO
Product code
Code GKP
Device class
Class 2
Regulation
21 CFR 864.5400
Advisory panel
Hematology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lexington, MA, US
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