510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925467Unknown

Jj Skinner Carekits(tm) Dry/wet/gel Skin Scrub Kit

J.J. Skinner, Inc., Great Neck NY / Traditional, Unknown
FDA source (opens on fda.gov)

K925467 is the FDA 510(k) clearance record for JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT, a class II device, cleared for J.J. Skinner, Inc. on under FDA product code LRO (General Surgery Tray). FDA's definition for product code LRO reads: "This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the...". FDA records list 7 510(k) clearances for J.J. Skinner, Inc., from to . As of , FDA records show no recalls naming K925467.

Clearance record

Decision date
Received
(559 days to decision)
Product code
LRO General Surgery Tray
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
J.J. Skinner, Inc. C/O Medical Device Inspection, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code LRO

Trailing 12 months

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

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