510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K863300Substantially Equivalent

Q101 Diagnostic Spirometer

Quinton, Inc., Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863300 is the FDA 510(k) clearance record for Q101 DIAGNOSTIC SPIROMETER, a class II device, cleared for Quinton, Inc. on under FDA product code BYT (Ventilator, External Body, Negative Pressure, Adult (Cuirass)). FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show no recalls naming K863300.

Clearance record

Decision date
Received
(80 days to decision)
Product code
BYT Ventilator, External Body, Negative Pressure, Adult (Cuirass)
Regulation
21 CFR 868.5935
Device class
Class II
Review panel
Anesthesiology
Applicant
Quinton, Inc. 2121 Terry Ave., Seattle WA
Third party review
No

Clearances, product code BYT

Trailing 12 months

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

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