510(k) K780857

MIXING BOWL & SPATULA, DISPOSABLE by Howmedica Corp. — Product Code JDZ

K780857 is an FDA 510(k) premarket notification submitted by Howmedica Corp. for the device "MIXING BOWL & SPATULA, DISPOSABLE". The FDA issued a decision of Substantially Equivalent on June 13, 1978. The device falls under product code JDZ (Mixer, Cement, For Clinical Use), a Class I device regulated under 21 CFR 888.4210. Howmedica Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1978
Date Received
May 24, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mixer, Cement, For Clinical Use
Device Class
Class I
Regulation Number
888.4210
Review Panel
OR
Submission Type