510(k) K882647
K882647 is an FDA 510(k) premarket notification submitted by Gesco Intl., Inc. for the device "GESCO CATHETERIZATION TRAY". The FDA issued a decision of Substantially Equivalent (with conditions) on September 9, 1988. The device falls under product code GBQ (Catheter, Continuous Irrigation), a Class I device regulated under 21 CFR 878.4200. Gesco Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESD (Substantially Equivalent (with conditions))
- Decision Date
- September 9, 1988
- Date Received
- June 27, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Continuous Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type