510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881790Substantially Equivalent

Safety Drain

Ballard Medical Products, Midvale UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881790 is the FDA 510(k) clearance record for SAFETY DRAIN, a class I device, cleared for Ballard Medical Products on under FDA product code BYH (Drain, Tee (Water Trap)). FDA records list 26 510(k) clearances for Ballard Medical Products, from to . As of , FDA records show no recalls naming K881790.

Clearance record

Decision date
Received
(56 days to decision)
Product code
BYH Drain, Tee (Water Trap)
Regulation
21 CFR 868.5995
Device class
Class I
Review panel
Anesthesiology
Applicant
Ballard Medical Products 6864 S. 300 W., Midvale UT
Third party review
No

Clearances, product code BYH

Trailing 12 months

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

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