510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K813390Substantially Equivalent

Bondary Single-Use or Gown

The Buckeye Cellulose Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813390 is the FDA 510(k) clearance record for BONDARY SINGLE-USE OR GOWN, a class II device, cleared for The Buckeye Cellulose Corp. on under FDA product code FYA (Gown, Surgical). FDA records list 18 510(k) clearances for The Buckeye Cellulose Corp., from to . As of , FDA records show no recalls naming K813390.

Clearance record

Decision date
Received
(33 days to decision)
Product code
FYA Gown, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
The Buckeye Cellulose Corp. 803 N. Front St. Suite 3, Mchenry IL
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