The following data is part of a premarket notification filed by Deschutes Medical Products, Inc. with the FDA for Pelvx Incontinence Dish, Model 301-306.
Device ID | K990593 |
510k Number | K990593 |
Device Name: | PELVX INCONTINENCE DISH, MODEL 301-306 |
Classification | Pessary, Vaginal |
Applicant | DESCHUTES MEDICAL PRODUCTS, INC. 1011 S.W. EMKAY DR., SUITE 104 Bend, OR 97702 |
Contact | Denise Bestwick |
Correspondent | Denise Bestwick DESCHUTES MEDICAL PRODUCTS, INC. 1011 S.W. EMKAY DR., SUITE 104 Bend, OR 97702 |
Product Code | HHW |
CFR Regulation Number | 884.3575 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-02-24 |
Decision Date | 1999-05-24 |
Summary: | summary |