510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811855Substantially Equivalent

Skin Scrub Kits

Oem Medical Div., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811855 is the FDA 510(k) clearance record for SKIN SCRUB KITS, a class I device, cleared for Oem Medical Div. on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 5 510(k) clearances for Oem Medical Div., from to . As of , FDA records show no recalls naming K811855.

Clearance record

Decision date
Received
(30 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Oem Medical Div. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

FDA records show no clearances under product code KDD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KDD, 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 20260
October 20260