510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K813263Substantially Equivalent

Patient Underpad

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

K813263 is the FDA 510(k) clearance record for PATIENT UNDERPAD, a class I device, cleared for The Buckeye Cellulose Corp. on under FDA product code KME (Bedding, Disposable, Medical). FDA records list 18 510(k) clearances for The Buckeye Cellulose Corp., from to . As of , FDA records show no recalls naming K813263.

Clearance record

Decision date
Received
(7 days to decision)
Product code
KME Bedding, Disposable, Medical
Regulation
21 CFR 880.6060
Device class
Class I
Review panel
General Hospital
Applicant
The Buckeye Cellulose Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KME

Trailing 12 months

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

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