510(k) K881736
K881736 is an FDA 510(k) premarket notification submitted by Medical Engineering Corp. for the device "SURGITEK CO2 DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on August 11, 1988. The device falls under product code FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic Device), a Class II device regulated under 21 CFR 876.1620. Medical Engineering Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 11, 1988
- Date Received
- April 22, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
- Device Class
- Class II
- Regulation Number
- 876.1620
- Review Panel
- GU
- Submission Type