Atlas FDA

PORTEX RING PESSARY PVC-NON STERILE; PORTEX RING PESSARY POLYTHENE- NON STERILE

FDA 510(k) clearance K012277 · decided 2002-02-11

Clearance details

K-number
K012277
Device name
PORTEX RING PESSARY PVC-NON STERILE; PORTEX RING PESSARY POLYTHENE- NON STERILE
Applicant
Sims Portex , Ltd.
Decision
Substantially Equivalent
Date received
2001-07-19
Decision date
2002-02-11
Days to decision
207 days
Clearance type
Traditional
Product code
HHW
Device class
2
Regulation number
884.3575
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Hythe, Kent, GB
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
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Uresta® (K233548)Resilia, Inc.2024-04-03
Gynethotics™ Pessary (K231786)Cosm Medical2024-03-06
ProVate Vaginal Support (K190277)Contipi Medical , Ltd.2019-07-08
Revive Reusable Bladder Support (K183468)Rinovum Subsidiary 2, LLC2019-01-25
Panpac Flexi Shelf Pessary (K173351)Panpac Medical Corporation2018-10-31
Panpac Disposable Pessary Fitting Set (K153422)Panpac Medical Corporation2016-07-14
Always/Tampax bladder supports (K151413)Procter & Gamble2015-12-18

Recalls involving this device

No recalls on record reference this clearance.