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
K870698Substantially Equivalent

Van-Tec Prostate Biopsy Needle

Van-Tec, Inc., Spencer IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870698 is the FDA 510(k) clearance record for VAN-TEC PROSTATE BIOPSY NEEDLE, a class I device, cleared for Van-Tec, Inc. on under FDA product code KNN (Components, Wheelchair). FDA records list 52 510(k) clearances for Van-Tec, Inc., from to . As of , FDA records show no recalls naming K870698.

Clearance record

Decision date
Received
(34 days to decision)
Product code
KNN Components, Wheelchair
Regulation
21 CFR 890.3920
Device class
Class I
Review panel
Physical Medicine
Applicant
Van-Tec, Inc. P.O. Box 26, Spencer IN
Third party review
No

Clearances, product code KNN

Trailing 12 months

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

FDA records show no clearances under product code KNN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNN, 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