510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811301Substantially Equivalent

Tubmate

American Stair-Glide Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811301 is the FDA 510(k) clearance record for TUBMATE, a class I device, cleared for American Stair-Glide Corp. on under FDA product code ILS (Adaptor, Hygiene). FDA records list 2 510(k) clearances for American Stair-Glide Corp., from to . As of , FDA records show no recalls naming K811301.

Clearance record

Decision date
Received
(16 days to decision)
Product code
ILS Adaptor, Hygiene
Regulation
21 CFR 890.5050
Device class
Class I
Review panel
Physical Medicine
Applicant
American Stair-Glide Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ILS

Trailing 12 months

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

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