HALE SUN SURGICAL TOWEL OR O.R. TOWEL— 510(k) K905803

Name: FDA 510(k) clearance K905803
Creator: U.S. Food and Drug Administration
Published: 1991-05-21

Substantially Equivalent

Hale Sun Industries, Ltd.

FDA 510(k) clearance K905803 for HALE SUN SURGICAL TOWEL OR O.R. TOWEL, Substantially Equivalent on 1991-05-21. Applicant: Hale Sun Industries, Ltd.. Device class: 2.

Clearance details

Applicant: Hale Sun Industries, Ltd.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1990-12-28
Decision date: 1991-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Providence, RI, US

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