RUSCH TRACHEAL BRONCHIAL Y STENT— 510(k) K953593

Name: FDA 510(k) clearance K953593
Creator: U.S. Food and Drug Administration
Published: 1995-10-13

Substantially Equivalent - Subject to Tracking Reg.

Rusch, Inc.

FDA 510(k) clearance K953593 for RUSCH TRACHEAL BRONCHIAL Y STENT, Substantially Equivalent - Subject to Tracking Reg. on 1995-10-13. Applicant: Rusch, Inc.. Device class: 2.

Clearance details

Applicant: Rusch, Inc.
Product code: Code NYT
Device class: Class 2
Regulation: 21 CFR 878.3720
Advisory panel: General, Plastic Surgery
Date received: 1995-07-31
Decision date: 1995-10-13
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Jeffrey, NH, US

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