Cleared Special

K020590 - MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER

K020590 is an FDA 510(k) clearance for MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER, manufactured by Getinge/Castle, Inc.. The device is a Class 2 General Hospital device with product code FLE cleared through the Special 510(k) pathway after a 26-day FDA review.

K020590 · Getinge/Castle, Inc. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2002
Decision
26d
Days
Class 2
Risk

K020590 is an FDA 510(k) clearance for the MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER. Classified as Sterilizer, Steam (product code FLE), Class II - Special Controls.

Submitted by Getinge/Castle, Inc. (Rochester, US). The FDA issued a Cleared decision on March 20, 2002 after a review of 26 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6880 - the FDA general hospital device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K020590

510(k) Number K020590 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 2002
Decision Date March 20, 2002
Days to Decision 26 days
Submission Type Special
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 129d · This submission: 26d
Pathway characteristics
Modification to existing cleared device.

FLE Device Classification - Class 2, Special Controls

Product Code FLE Sterilizer, Steam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6880
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 - FLE Sterilizer, Steam

All 171
Devices cleared under the same product code (FLE) and FDA review panel - the closest regulatory comparables to K020590.
TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
K021504 · Tuttnauer U.S.A Co, Ltd. · Jul 2002
BELIMED STEAM STERILIZER, MODEL TOP 5000
K021223 · Sauter AG · Jun 2002
AMSCO CENTURY MEDIUM STERILIZER 26 X 26
K020747 · STERIS Corporation · May 2002
HARVEY PV DRY STERILIZER, MODEL # ST127325
K014174 · Barnstead/Thermolyne Corp. · Feb 2002
CASTLE 400HC/500HC SERIES STEAM STERILIZER, MODELS 422HC, 433HC, 522HC, AND 533HC
K012573 · Getinge/Castle, Inc. · Sep 2001
AMSCO CENTURY MEDIUM STERILIZER, MODEL CENTURY
K010865 · STERIS Corporation · May 2001
K020590 · MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER
Download PDF FDA Summary Getinge/Castle, Inc.