510(k) K881826
K881826 is an FDA 510(k) premarket notification submitted by The Hygenic Corp. for the device "ENDO-ICE". The FDA issued a decision of SN on August 23, 1988. The device falls under product code EAT (Tester, Pulp), a Class II device regulated under 21 CFR 872.1720. The Hygenic Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- August 23, 1988
- Date Received
- April 29, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tester, Pulp
- Device Class
- Class II
- Regulation Number
- 872.1720
- Review Panel
- DE
- Submission Type