510(k) K801651

CUTTER JET by Cutter Laboratories, Inc. — Product Code EFB

K801651 is an FDA 510(k) premarket notification submitted by Cutter Laboratories, Inc. for the device "CUTTER JET". The FDA issued a decision of Substantially Equivalent on August 13, 1980. The device falls under product code EFB (Handpiece, Air-Powered, Dental), a Class I device regulated under 21 CFR 872.4200. Cutter Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 13, 1980
Date Received
July 18, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Handpiece, Air-Powered, Dental
Device Class
Class I
Regulation Number
872.4200
Review Panel
DE
Submission Type