510(k) K790275

GUN, EXETER CEMENT by Howmedica Corp. — Product Code KIH

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