Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K970589Substantially Equivalent

Microetcher Ap

Danville Engineering, Inc., San Ramon CA / Traditional, Substantially Equivalent

K970589 is the FDA 510(k) clearance record for MICROETCHER AP, a class II device, cleared for Danville Engineering, Inc. on under FDA product code KOJ (Airbrush). FDA records list 4 510(k) clearances for Danville Engineering, Inc., from to . As of , FDA records show no recalls naming K970589.

Clearance record

Decision date
Received
(211 days to decision)
Product code
KOJ Airbrush
Regulation
21 CFR 872.6080
Device class
Class II
Review panel
Dental
Applicant
Danville Engineering, Inc. 2021 Omega Dr., San Ramon CA
510(k) summary
Statement
Third party review
No

Clearances, product code KOJ

Trailing 12 months

FDA records hold no clearances under product code KOJ in the trailing twelve months.

FDA records show no clearances under product code KOJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KOJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260