510(k) K790275
K790275 is an FDA 510(k) premarket notification submitted by Howmedica Corp. for the device "GUN, EXETER CEMENT". The FDA issued a decision of Substantially Equivalent on February 21, 1979. The device falls under product code KIH (Dispenser, Cement), a Class I device regulated under 21 CFR 888.4200. Howmedica Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 21, 1979
- Date Received
- February 9, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dispenser, Cement
- Device Class
- Class I
- Regulation Number
- 888.4200
- Review Panel
- OR
- Submission Type