Cleared Abbreviated

K023083 - SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800

K023083 is an FDA 510(k) clearance for SILBERG T.P.S., manufactured by Mettler Electronics Corp.. The device is a Class 2 General Hospital device with product code FRN cleared through the Abbreviated 510(k) pathway after a 164-day FDA review.

K023083 · Mettler Electronics Corp. · General Hospital
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Feb 2003
Decision
164d
Days
Class 2
Risk

K023083 is an FDA 510(k) clearance for the SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Mettler Electronics Corp. (Anaheim, US). The FDA issued a Cleared decision on February 28, 2003 after a review of 164 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - the FDA general hospital device 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 Mettler Electronics Corp. devices

FDA 510(k) Submission Details - K023083

510(k) Number K023083 FDA.gov
FDA Decision Cleared Substantially Equivalent - Third Party Review (ST)
Date Received September 17, 2002
Decision Date February 28, 2003
Days to Decision 164 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
35d slower than avg
Panel avg: 129d · This submission: 164d
Pathway characteristics
Standards-based clearance path.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 General Hospital devices follow this clearance model.

Regulatory Peers - FRN Pump, Infusion

All 582
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K023083.
MEDLEY SYSTEM WITH MEDICATION MANAGEMENT SYSTEM (MMS)
K030459 · Alaris Medical Systems, Inc. · Apr 2003
VISTA BASIC WITH FM SYSTEM
K023189 · B.Braun Medical, Inc. · Mar 2003
FENESTRATED INFUSION CATHETER
K024190 · Promedic, Inc. · Mar 2003
ABBOTT PLUM A+ INFUSION PUMP, MODEL 12391
K024084 · Abbott Laboratories · Dec 2002
MEDLEY SYRINGE PUMP MODULE SYSTEM, MODEL 8110
K023264 · Alaris Medical Systems, Inc. · Dec 2002
PARAGON INFUSION SYSTEM WITH BOLUS
K023827 · I-Flow Corp. · Dec 2002