510(k) K790244
K790244 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "CYSTOTOMES". The FDA issued a decision of Substantially Equivalent on February 12, 1979. The device falls under product code HNY (Cystotome), a Class I device regulated under 21 CFR 886.4350. Visitec Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 12, 1979
- Date Received
- December 29, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cystotome
- Device Class
- Class I
- Regulation Number
- 886.4350
- Review Panel
- OP
- Submission Type