510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K882739Substantially Equivalent

Intertech Large Volume Water Trap (Lvw)

Intertech Resources, Inc., Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882739 is the FDA 510(k) clearance record for INTERTECH LARGE VOLUME WATER TRAP (LVW), a class I device, cleared for Intertech Resources, Inc. on under FDA product code BYH (Drain, Tee (Water Trap)). FDA records list 29 510(k) clearances for Intertech Resources, Inc., from to . As of , FDA records show no recalls naming K882739.

Clearance record

Decision date
Received
(39 days to decision)
Product code
BYH Drain, Tee (Water Trap)
Regulation
21 CFR 868.5995
Device class
Class I
Review panel
Anesthesiology
Applicant
Intertech Resources, Inc. 333 W. Wacker Dr., Chicago IL
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