510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K851798Substantially Equivalent

53-160 to 53-167 Various Biopsy Forceps Yeoman

Artiberia, San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851798 is the FDA 510(k) clearance record for 53-160 TO 53-167 VARIOUS BIOPSY FORCEPS YEOMAN, a class II device, cleared for Artiberia on under FDA product code KNW (Instrument, Biopsy). FDA records list 79 510(k) clearances for Artiberia, from to . As of , FDA records show no recalls naming K851798.

Clearance record

Decision date
Received
(28 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Artiberia 4518 Los Ranchitos, San Antonio TX
Third party review
No

Clearances, product code KNW

Trailing 12 months
8 clearances under product code KNW in the twelve months to October 2026, August 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code KNW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20260
August 20264
September 20260
October 20260