Pelvx Incontinence Dish, Model 301-306

FDA 510(k) K990593 · Deschutes Medical Products, Inc.

Substantially Equivalent

510(k) numberK990593

Submission

Device name
Pelvx Incontinence Dish, Model 301-306
Applicant
Deschutes Medical Products, Inc.
Bend, OR, US
Received
February 24, 1999
Decision date
May 24, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HHW – Pessary, Vaginal
Device class
Class II (moderate risk)
Regulation
21 CFR 884.3575
Specialty
Obstetrics/Gynecology

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K253698Milex™ Incontinence Dish Pessaries; Milex™ Incontinence Dish Pessaries with Support…HHW · Traditional Cooper Surgical01/20/2026SE
K250438CooperSurgical Milex® PessariesHHW · Traditional CooperSurgical, Inc.04/11/2025SE
K240798Cntrl+ Bladder Support PessaryHHW · Traditional Cntrl+, Inc.12/17/2024SE
K232677Reia pessaryHHW · Traditional Reia, LLC05/21/2024SE
K232525Yoni.Fit Bladder SupportHHW · Traditional Watkins-Conti Products, Inc.05/17/2024SE
K233548Uresta®HHW · Traditional Resilia, Inc.04/03/2024SE
K231786Gynethotics™ PessaryHHW · Traditional Cosm Medical03/06/2024SE
K190277ProVate Vaginal SupportHHW · Traditional Contipi Medical , Ltd.07/08/2019SE
K183468Revive Reusable Bladder SupportHHW · Traditional Rinovum Subsidiary 2, LLC01/25/2019SE
K173351Panpac Flexi Shelf PessaryHHW · Abbreviated Panpac Medical Corporation10/31/2018SE

More from Panpac Medical Corporation

510(k)DeviceDecision
K002329Pelvx Gellhorn Vaginal Pessary 603-608HHW · Traditional 09/18/2000SE
K994079Reflex Treatment SystemHIR · Traditional 03/01/2000SE
K974117Pelvx Donut, Pelvx CubeHHW · Traditional 04/27/1998SE
K974116Pelvx Incontinence RingHHW · Traditional 04/27/1998SE
K974115Pelvx Ring, Pelvx Ring with SupportHHW · Traditional 04/27/1998SE
K934552PeripumpHIR · Traditional 08/09/1995SE
K951569SurgactivatorLJH · Traditional 06/06/1995SE

Questions and answers

When was Pelvx Incontinence Dish, Model 301-306 cleared by the FDA?

Pelvx Incontinence Dish, Model 301-306 (K990593) received a 510(k) decision of Substantially Equivalent on May 24, 1999, 89 days after the submission was received.

What is the product code of K990593?

The FDA product code is HHW – Pessary, Vaginal, a Class II (moderate risk) device regulated under 21 CFR 884.3575.