MANOMETER— 510(k) K122077

Substantially Equivalent

Intersurgical, Inc.

FDA 510(k) clearance K122077 for MANOMETER, Substantially Equivalent on 2013-01-10. Applicant: Intersurgical, Inc.. Device class: 2.

Clearance details

Applicant
Intersurgical, Inc.
Product code
Code CAP
Device class
Class 2
Regulation
21 CFR 868.2600
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Liverpool, NY, US
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