510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932722Substantially Equivalent

Carie Med-Tech Model 210 Rainout Drainage System

Carie Med-Tech Services, Inc., Olney IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932722 is the FDA 510(k) clearance record for CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM, a class I device, cleared for Carie Med-Tech Services, Inc. on under FDA product code BYH (Drain, Tee (Water Trap)). FDA records list one 510(k) clearance for Carie Med-Tech Services, Inc. As of , FDA records show no recalls naming K932722.

Clearance record

Decision date
Received
(63 days to decision)
Product code
BYH Drain, Tee (Water Trap)
Regulation
21 CFR 868.5995
Device class
Class I
Review panel
Anesthesiology
Applicant
Carie Med-Tech Services, Inc. P.O. Box 449, Olney IL
510(k) summary
Statement
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