Atlas FDA

WORRY-REMOVER IRRIGATOR

FDA 510(k) clearance K030056 · decided 2003-04-22

Clearance details

K-number
K030056
Device name
WORRY-REMOVER IRRIGATOR
Applicant
Corisen Group, Ltd.
Decision
Substantially Equivalent
Date received
2003-01-06
Decision date
2003-04-22
Days to decision
106 days
Clearance type
Traditional
Product code
HED
Device class
1
Regulation number
884.5900
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
West Chester, OH, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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FEMININE HYGIENE DEVICE (K831667)Snow Willow Co.1983-09-12
DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID (K800954)The Healthcare Group Laboratories, Inc.1980-10-03
DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN (K800956)The Healthcare Group Laboratories, Inc.1980-10-03
DOUCHE UNIT-1500 ML DISP. CONTAINER (K800957)The Healthcare Group Laboratories, Inc.1980-07-14
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Recalls involving this device

No recalls on record reference this clearance.