510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932456Substantially Equivalent

Jarit Surgical Instruments

J. Jamner Surgical Instruments, Inc., Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932456 is the FDA 510(k) clearance record for JARIT SURGICAL INSTRUMENTS, a class II device, cleared for J. Jamner Surgical Instruments, Inc. on under FDA product code KNF (Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)). FDA records list 11 510(k) clearances for J. Jamner Surgical Instruments, Inc., from to . As of , FDA records show one recall naming K932456.

Clearance record

Decision date
Received
(335 days to decision)
Product code
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Regulation
21 CFR 884.4160
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
J. Jamner Surgical Instruments, Inc. 55 Northern Blvd., Suite 301, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code KNF

Trailing 12 months
1 clearance under product code KNF in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KNF, 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 20261
October 20260