510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K813382Substantially Equivalent

Disposable Adult Anes. Circuit

Intec., Blue Springs MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813382 is the FDA 510(k) clearance record for DISPOSABLE ADULT ANES. CIRCUIT, a class I device, cleared for Intec. on under FDA product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)). FDA records list 3 510(k) clearances for Intec., from to . As of , FDA records show no recalls naming K813382.

Clearance record

Decision date
Received
(51 days to decision)
Product code
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)
Regulation
21 CFR 868.5240
Device class
Class I
Review panel
Anesthesiology
Applicant
Intec. 22200 E. 40 Hwy., Blue Springs MO
Third party review
No

Clearances, product code CAI

Trailing 12 months

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

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