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
K932812Substantially Equivalent

Ec 5R Plethysmograph

D. E. Hokanson, Inc., Bellevue WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932812 is the FDA 510(k) clearance record for EC 5R PLETHYSMOGRAPH, a class II device, cleared for D. E. Hokanson, Inc. on under FDA product code JEH (Plethysmograph, Volume). FDA records list 19 510(k) clearances for D. E. Hokanson, Inc., from to . As of , FDA records show no recalls naming K932812.

Clearance record

Decision date
Received
(218 days to decision)
Product code
JEH Plethysmograph, Volume
Regulation
21 CFR 868.1760
Device class
Class II
Review panel
Anesthesiology
Applicant
D. E. Hokanson, Inc. 12840 NE 21st Pl., Bellevue WA
510(k) summary
Statement
Third party review
No

Clearances, product code JEH

Trailing 12 months

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

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