MASTERLAB PFT AND MASTERLAB BODY BOX— 510(k) K893420

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K893420 for MASTERLAB PFT AND MASTERLAB BODY BOX, Substantially Equivalent on 1989-06-23. Applicant: Quinton, Inc.. Device class: 2.

Clearance details

Applicant
Quinton, Inc.
Product code
Code CCM
Device class
Class 2
Regulation
21 CFR 868.1750
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Seattle, WA, US
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