Cleared Abbreviated

K032608 - GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETER

K032608 is an FDA 510(k) clearance for GONOTEC CALIBRATION SOLUTION 300 MOSMOL..., manufactured by Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB. The device is a Class 2 Chemistry device with product code JIS cleared through the Abbreviated 510(k) pathway after a 57-day FDA review.

K032608 · Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2003
Decision
57d
Days
Class 2
Risk

K032608 is an FDA 510(k) clearance for the GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETER. Classified as Calibrator, Primary (product code JIS), Class II - Special Controls.

Submitted by Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB (Berlin, DE). The FDA issued a Cleared decision on October 21, 2003 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - the FDA in vitro diagnostics and chemistry framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB devices

FDA 510(k) Submission Details - K032608

510(k) Number K032608 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 25, 2003
Decision Date October 21, 2003
Days to Decision 57 days
Submission Type Abbreviated
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d faster than avg
Panel avg: 88d · This submission: 57d
Pathway characteristics
Standards-based clearance path.

JIS Device Classification - Class 2, Special Controls

Product Code JIS Calibrator, Primary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JIS Calibrator, Primary

All 113
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