510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K984415Substantially Equivalent

S.s. White Technologies, Models 6500-D,6500-E, and 6500-F

S.S. White Technologies, Inc., Piscataway NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K984415 is the FDA 510(k) clearance record for S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F, a class II device, cleared for S.S. White Technologies, Inc. on under FDA product code KOJ (Airbrush). FDA records list one 510(k) clearance for S.S. White Technologies, Inc. As of , FDA records show no recalls naming K984415.

Clearance record

Decision date
Received
(293 days to decision)
Product code
KOJ Airbrush
Regulation
21 CFR 872.6080
Device class
Class II
Review panel
Dental
Applicant
S.S. White Technologies, Inc. 151 Old New Brunswick Rd., Piscataway NJ
510(k) summary
Summary
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