DILULAB 230— 510(k) K823522

Substantially Equivalent

Innovative Medical Systems, Inc.

FDA 510(k) clearance K823522 for DILULAB 230, Substantially Equivalent on 1982-12-28. Applicant: Innovative Medical Systems, Inc.. Device class: 1.

Clearance details

Applicant: Innovative Medical Systems, Inc.
Product code: Code GKH
Device class: Class 1
Regulation: 21 CFR 864.5240
Advisory panel: Hematology
Date received: 1982-11-29
Decision date: 1982-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GKH

K100684 — CELLTRACKS AUTOPREP SYSTEM MODEL:95412010-08-26
K040077 — IMMUNICON CELLTRACKS AUTOPREP SYSTEM2004-03-12
K022512 — CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 95182002-09-30
K021150 — COULTER CELLPREP2002-06-11
K935953 — COULTER MULTI Q PREP1994-03-11

More clearances from Innovative Medical Systems, Inc.

K973035 — VIOLA II DENTAL CAMERA SYSTEM1997-09-24
K951469 — BAZOOKA SYSTEM1995-06-28
K933184 — POSITIVE AIRWAY PRESSURE SYSTEM1994-11-28
K924590 — MICROWAVE AUTOMATED TISSUE PROCESSOR1992-12-29
K922081 — LABOTECH AUTOMATED MICROTITER ANALYZER1992-09-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.