PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES— 510(k) K905462

Name: FDA 510(k) clearance K905462
Creator: U.S. Food and Drug Administration
Published: 1991-02-06

Substantially Equivalent

Angiosystems, Inc.

FDA 510(k) clearance K905462 for PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES, Substantially Equivalent on 1991-02-06. Applicant: Angiosystems, Inc.. Device class: 1.

Clearance details

Applicant: Angiosystems, Inc.
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-12-05
Decision date: 1991-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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K905461 — PROCEDURE KIT/ROUTINE DENTAL PROCEDURES1991-03-05
K905465 — STERILE DISPOS SURGICAL DRAPE/C-SECTION DRAPE1991-02-11
K905466 — STERILE DISPOSABLE SURGICAL DRAPE/ABDOMINAL DRAPE1991-02-11

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