BTP(TM) CENTRALINE(TM) SUIT— 510(k) K914615

Name: FDA 510(k) clearance K914615
Creator: U.S. Food and Drug Administration
Published: 1992-05-05

Substantially Equivalent

Btp Industries, Inc.

FDA 510(k) clearance K914615 for BTP(TM) CENTRALINE(TM) SUIT, Substantially Equivalent on 1992-05-05. Applicant: Btp Industries, Inc.. Device class: 1.

Clearance details

Applicant: Btp Industries, Inc.
Product code: Code FXO
Device class: Class 1
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1991-10-17
Decision date: 1992-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: S. Hamilton, MA, US

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