510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011329Substantially Equivalent

Eccovision Acoustic Diagnostic Imaging Acoustic Pharyngometer

E. Benson Hood Lab, Inc., Pembroke MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011329 is the FDA 510(k) clearance record for ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETER, a class II device, cleared for E. Benson Hood Lab, Inc. on under FDA product code BXQ (Rhinoanemometer (Measurement Of Nasal Decongestion)). FDA records list 3 510(k) clearances for E. Benson Hood Lab, Inc., from to . As of , FDA records show no recalls naming K011329.

Clearance record

Decision date
Received
(451 days to decision)
Product code
BXQ Rhinoanemometer (Measurement Of Nasal Decongestion)
Regulation
21 CFR 868.1800
Device class
Class II
Review panel
Anesthesiology
Applicant
E. Benson Hood Lab, Inc. 575 Washington St., Pembroke MA
510(k) summary
Summary
Third party review
No

Clearances, product code BXQ

Trailing 12 months

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

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