510(k) K023017
K023017 is an FDA 510(k) premarket notification submitted by Fertility Technology Resources, Inc. for the device "TUCKER EMBRYO CATHETER". The FDA issued a decision of Substantially Equivalent on December 13, 2002. The device falls under product code MQF (Catheter, Assisted Reproduction), a Class II device regulated under 21 CFR 884.6110. Fertility Technology Resources, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 13, 2002
- Date Received
- September 10, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Assisted Reproduction
- Device Class
- Class II
- Regulation Number
- 884.6110
- Review Panel
- OB
- Submission Type