HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT— 510(k) K953544

Substantially Equivalent

Gibeck, Inc.

FDA 510(k) clearance K953544 for HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT, Substantially Equivalent on 1995-08-25. Applicant: Gibeck, Inc.. Device class: 1.

Clearance details

Applicant
Gibeck, Inc.
Product code
Code BYD
Device class
Class 1
Regulation
21 CFR 868.5375
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Indianapolis, IN, US
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