RESPISOMNOGRAPH— 510(k) K861326

Substantially Equivalent

Dickstein, Shapiro & Morin

FDA 510(k) clearance K861326 for RESPISOMNOGRAPH, Substantially Equivalent on 1986-06-13. Applicant: Dickstein, Shapiro & Morin. Device class: 2.

Clearance details

Applicant
Dickstein, Shapiro & Morin
Product code
Code BZQ
Device class
Class 2
Regulation
21 CFR 868.2375
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
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