TURKEL PNEUMOTHORAX KIT— 510(k) K923028

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K923028 for TURKEL PNEUMOTHORAX KIT, Substantially Equivalent on 1992-08-04. Applicant: Symbiosis Corp.. Device class: 1.

Clearance details

Applicant: Symbiosis Corp.
Product code: Code GCB
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1992-06-23
Decision date: 1992-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.