510(k) K864964
K864964 is an FDA 510(k) premarket notification submitted by Medovations, Inc. for the device "5 - IN - 1 CONNECTOR". The FDA issued a decision of Substantially Equivalent on January 20, 1987. The device falls under product code GAZ (Tubing, Noninvasive), a Class II device regulated under 21 CFR 880.6740. Medovations, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 20, 1987
- Date Received
- December 22, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubing, Noninvasive
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type