510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K930167Substantially Equivalent

Reusable Towel and Gown Packs

Custom Sterile Services, Inc., Tumwater WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930167 is the FDA 510(k) clearance record for REUSABLE TOWEL AND GOWN PACKS, a class II device, cleared for Custom Sterile Services, Inc. on under FDA product code FYD (Apparatus, Exhaust, Surgical). FDA records list one 510(k) clearance for Custom Sterile Services, Inc. As of , FDA records show no recalls naming K930167.

Clearance record

Decision date
Received
(321 days to decision)
Product code
FYD Apparatus, Exhaust, Surgical
Regulation
21 CFR 878.5070
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Custom Sterile Services, Inc. 711 - 78th Ave. SW, Tumwater WA
510(k) summary
Statement
Third party review
No

Clearances, product code FYD

Trailing 12 months

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

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