510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790049Substantially Equivalent

Bed, Paraplegic

Wayne V. Kirkman, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790049 is the FDA 510(k) clearance record for BED, PARAPLEGIC, a class II device, cleared for Wayne V. Kirkman on under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital). FDA records list one 510(k) clearance for Wayne V. Kirkman. As of , FDA records show no recalls naming K790049.

Clearance record

Decision date
Received
(49 days to decision)
Product code
FNL Bed, Ac-Powered Adjustable Hospital
Regulation
21 CFR 880.5100
Device class
Class II
Review panel
General Hospital
Applicant
Wayne V. Kirkman 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FNL

Trailing 12 months

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

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