510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K093896Substantially Equivalent

Ethicon Endo Surgery Slotted Anoscope

Ethicon Endo-Surgery Inc, Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093896 is the FDA 510(k) clearance record for ETHICON ENDO SURGERY SLOTTED ANOSCOPE, a class II device, cleared for Ethicon Endo-Surgery, Inc. on under FDA product code FER (Anoscope And Accessories). FDA's definition for product code FER reads: "To examine and perform procedures within the anus and rectum". FDA records list 185 510(k) clearances for Ethicon Endo-Surgery, Inc., from to . As of , FDA records show no recalls naming K093896.

Clearance record

Decision date
Received
(97 days to decision)
Product code
FER Anoscope And Accessories
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Ethicon Endo-Surgery, Inc. 4545 Creek Rd., Cincinnati OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FER

Trailing 12 months

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

FDA records show no clearances under product code FER in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FER, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260