SURGISTAR BLADES— 510(k) K923689

Substantially Equivalent

Surgistar, Inc.

FDA 510(k) clearance K923689 for SURGISTAR BLADES, Substantially Equivalent on 1992-09-09. Applicant: Surgistar, Inc.. Device class: 1.

Clearance details

Applicant: Surgistar, Inc.
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-07-24
Decision date: 1992-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GDX

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K905380 — 1-CUT ACL GRAFT KNIFE1990-12-13
K895682 — VESSEL LOOPS1989-10-24

More clearances from Surgistar, Inc.

K030891 — SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK2003-06-17
K992978 — RICROKERATOME BLADE1999-11-16
K941747 — SURGISTAR TROCARS1994-07-01

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