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
K890432Substantially Equivalent

Deknatel High Precision Vascular Punch(tm)

Deknatel, Inc., San Jose-Heredia, CR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890432 is the FDA 510(k) clearance record for DEKNATEL HIGH PRECISION VASCULAR PUNCH(TM), a class I device, cleared for Deknatel, Inc. on under FDA product code DWS (Instruments, Surgical, Cardiovascular). FDA records list 37 510(k) clearances for Deknatel, Inc., from to . As of , FDA records show no recalls naming K890432.

Clearance record

Decision date
Received
(76 days to decision)
Product code
DWS Instruments, Surgical, Cardiovascular
Regulation
21 CFR 870.4500
Device class
Class I
Review panel
Cardiovascular
Applicant
Deknatel, Inc. Kilometer 9 Carretera, San Jose-Heredia, CR
Third party review
No

Clearances, product code DWS

Trailing 12 months

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

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