Cleared Traditional

K003068 - SAVINA

K003068 is an FDA 510(k) clearance for SAVINA, manufactured by Drager Medizintechnik GmbH. The device is a Class 2 Anesthesiology device with product code CBK cleared through the Traditional 510(k) pathway after a 266-day FDA review.

K003068 · Drager Medizintechnik GmbH · Anesthesiology device
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Jun 2001
Decision
266d
Days
Class 2
Risk

K003068 is an FDA 510(k) clearance for the SAVINA. Classified as Ventilator, Continuous, Facility Use (product code CBK), Class II - Special Controls.

Submitted by Drager Medizintechnik GmbH (Telford, US). The FDA issued a Cleared decision on June 25, 2001 after a review of 266 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5895 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Drager Medizintechnik GmbH devices

FDA 510(k) Submission Details - K003068

510(k) Number K003068 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 2000
Decision Date June 25, 2001
Days to Decision 266 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
126d slower than avg
Panel avg: 140d · This submission: 266d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CBK Device Classification - Class 2, Special Controls

Product Code CBK Ventilator, Continuous, Facility Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5895
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - CBK Ventilator, Continuous, Facility Use

All 357
Devices cleared under the same product code (CBK) and FDA review panel - the closest regulatory comparables to K003068.
AVEA
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SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407E
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BIRD TBIRD LEGACY VENTILATOR
K003770 · Bird Products Corp. · Dec 2000
PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION
K001646 · Puritan Bennett Corp. · Oct 2000
ACHIEVA VENTILATOR Y-ACH+E, ACHIEVA PS VENTILATOR Y-ACHPS+E, ACHIEVA PSO2 VENTILATOR Y-ACHPS02+E
K002686 · Nellcor Puritan Bennett, Inc. · Oct 2000