MODIFIED NOFLO I— 510(k) K871262

Substantially Equivalent

Design Technologies, Inc.

FDA 510(k) clearance K871262 for MODIFIED NOFLO I, Substantially Equivalent on 1987-07-21. Applicant: Design Technologies, Inc.. Device class: 1.

Clearance details

Applicant
Design Technologies, Inc.
Product code
Code CCN
Device class
Class 1
Regulation
21 CFR 868.2300
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Rahway, NJ, US
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