510(k) K935077
K935077 is an FDA 510(k) premarket notification submitted by Universal Medical Instrument Corp. for the device "CATH-SEAL". The FDA issued a decision of Substantially Equivalent on June 7, 1994. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Universal Medical Instrument Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 7, 1994
- Date Received
- October 22, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type