510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K873521Substantially Equivalent

Bronchodilator Tee - 9056 Series

Boehringer Laboratories, LLC, Norristown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873521 is the FDA 510(k) clearance record for BRONCHODILATOR TEE - 9056 SERIES, a class II device, cleared for Boehringer Laboratories on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 44 510(k) clearances for Boehringer Laboratories, from to . As of , FDA records show no recalls naming K873521.

Clearance record

Decision date
Received
(183 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Boehringer Laboratories P.O. Box 870, Norristown PA
Third party review
No

Clearances, product code CAF

Trailing 12 months
4 clearances under product code CAF in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAF, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260