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
K860593Substantially Equivalent

Et/rt Papillotome

Hobbs Medical, Inc., Stafford Springs CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860593 is the FDA 510(k) clearance record for ET/RT PAPILLOTOME, a class II device, cleared for Hobbs Medical, Inc. on under FDA product code KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories)). FDA records list 21 510(k) clearances for Hobbs Medical, Inc., from to . As of , FDA records show no recalls naming K860593.

Clearance record

Decision date
Received
(153 days to decision)
Product code
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Hobbs Medical, Inc. P.O. Box 46, Stafford Springs CT
Third party review
No

Clearances, product code KNS

Trailing 12 months
4 clearances under product code KNS in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KNS, trailing twelve months
MonthClearances
November 20252
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260