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
K241897Substantially Equivalent

Mor

Morari, Inc., Maple Grove MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K241897 is the FDA 510(k) clearance record for MOR, a class II device, cleared for Morari, Inc. on under FDA product code QRC (Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation). FDA's definition for product code QRC reads: "A non-implanted electrical stimulation device for management of premature ejaculation is intended to be used in patients with premature ejaculation by delivery of electrical stimulation to the perineal muscles and nerves". FDA records list one 510(k) clearance for Morari, Inc. As of , FDA records show no recalls naming K241897.

Clearance record

Decision date
Received
(228 days to decision)
Product code
QRC Non-Implanted Electrical Stimulation Device For Management Of Premature Ejaculation
Regulation
21 CFR 876.5026
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Morari, Inc. 6501 Zircon Ln., Maple Grove MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QRC

Trailing 12 months
1 clearance under product code QRC in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QRC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260