510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K133786Substantially Equivalent

Dornoch Duo Suction Cart with: Dl2800 Lid, Cl500 Lid, Dornoch Quad Suction Cart with: Dl2800 Lid, Cl500 Lid

Dornoch Medical Systems, Riverside MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133786 is the FDA 510(k) clearance record for DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID, a class II device, cleared for Dornoch Medical Systems, Inc. on under FDA product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered). FDA records list 6 510(k) clearances for Dornoch Medical Systems, Inc., from to . As of , FDA records show no recalls naming K133786.

Clearance record

Decision date
Received
(99 days to decision)
Product code
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
Regulation
21 CFR 878.4780
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Dornoch Medical Systems, Inc. 200 NW Pkwy. Rd., Riverside MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JCX

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