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Urologix, Inc.

6 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Prostiva RF Therapy Hand Piece Kit, REF 8929, Rx only, sterilized using Ethylene Oxide. Th recall (Z-0182-2014)Urologix, Inc.2013-11-08
The following kits contain the UROLOGIX, Coolant Bag, CA1111B, Sterile EO, Manufactured fo recall (Z-2710-2011)Urologix, Inc.2011-06-30
UROLOGIX CTC Advance" Standard Microwave Catheter (3.0-5.0 cm), CTC Advance" Long Microwav recall (Z-1174-2010)Urologix, Inc.2010-03-19
Urologix Microwave Delivery System 3.0 - 5.0. For use with prostatic urethra lengths of 3. recall (Z-0720-2007)Urologix, Inc.2007-04-05
Urologix Microwave Delivery System 2.5 - 3.5 For use with prostatic urethra lengths of 2.5 recall (Z-0721-2007)Urologix, Inc.2007-04-05
Prostatron Praktis Type II for Transurethral Microwave Thermotherapy. The Prostatron is a recall (Z-0345-04)Urologix, Inc.2004-07-20

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Every clearance here is in the API, with alerts when new ones post.