PNEUMOTHERML, MODEL: 5800— 510(k) K092685

Substantially Equivalent

Salter Labs

FDA 510(k) clearance K092685 for PNEUMOTHERML, MODEL: 5800, Substantially Equivalent on 2009-11-24. Applicant: Salter Labs. Device class: 2.

Clearance details

Applicant
Salter Labs
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
Special
Location
Arvin, CA, US
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