510(k) K030056
K030056 is an FDA 510(k) premarket notification submitted by Corisen Group, Ltd. for the device "WORRY-REMOVER IRRIGATOR". The FDA issued a decision of Substantially Equivalent on April 22, 2003. The device falls under product code HED (Douche Apparatus, Vaginal, Therapeutic), a Class I device regulated under 21 CFR 884.5900.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 22, 2003
- Date Received
- January 6, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Douche Apparatus, Vaginal, Therapeutic
- Device Class
- Class I
- Regulation Number
- 884.5900
- Review Panel
- OB
- Submission Type