510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851559Substantially Equivalent

Turquoise

Roseburg SA, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851559 is the FDA 510(k) clearance record for TURQUOISE, a class II device, cleared for Roseburg SA on under FDA product code FYA (Gown, Surgical). FDA records list 24 510(k) clearances for Roseburg SA, from to . As of , FDA records show no recalls naming K851559.

Clearance record

Decision date
Received
(14 days to decision)
Product code
FYA Gown, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Roseburg SA 1054 31st St., NW, Washington DC
Third party review
No

Clearances, product code FYA

Trailing 12 months
10 clearances under product code FYA in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FYA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20262
March 20260
April 20262
May 20261
June 20261
July 20261
August 20262
September 20260
October 20260