510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K874807Unknown

Extravakit

Cancer Technologies, Inc., Tucson AZ / Traditional, Unknown
FDA source (opens on fda.gov)

K874807 is the FDA 510(k) clearance record for EXTRAVAKIT, a class II device, cleared for Cancer Technologies, Inc. on under FDA product code FMF (Syringe, Piston). FDA records list 4 510(k) clearances for Cancer Technologies, Inc., from to . As of , FDA records show no recalls naming K874807.

Clearance record

Decision date
Received
(76 days to decision)
Product code
FMF Syringe, Piston
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Cancer Technologies, Inc. P.O. Box 12865, Tucson AZ
Third party review
No

Clearances, product code FMF

Trailing 12 months
14 clearances under product code FMF in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FMF, trailing twelve months
MonthClearances
November 20251
December 20254
January 20260
February 20261
March 20260
April 20261
May 20261
June 20262
July 20261
August 20263
September 20260
October 20260