RETIC-QUINOX— 510(k) K993496

Substantially Equivalent

Hematronix, Inc.

FDA 510(k) clearance K993496 for RETIC-QUINOX, Substantially Equivalent on 1999-11-30. Applicant: Hematronix, Inc.. Device class: 2.

Clearance details

Applicant: Hematronix, Inc.
Product code: Code JPK
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1999-10-15
Decision date: 1999-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Benicia, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Hematronix, Inc.

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K960471 — TRI-COUNT 201996-03-20
K960005 — TRI-COURT 20-T1996-03-19
K941965 — EZ-RANGE1995-04-25

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