MICRO BLADE II— 510(k) K812526

Substantially Equivalent

Vxtra Corp.

FDA 510(k) clearance K812526 for MICRO BLADE II, Substantially Equivalent on 1981-09-16. Applicant: Vxtra Corp.. Device class: 1.

Clearance details

Applicant: Vxtra Corp.
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-09-02
Decision date: 1981-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vxtra Corp.

K832938 — OCUTOME PARATUBING SET1983-10-19
K832980 — VXTRA OCUTOME KIT1983-10-19
K831266 — MICROSURGICAL KNIFE1983-06-10
K830379 — PHAKO KIT1983-04-05
K830385 — IRRIGATION/ASPIRATION KIT1983-04-05

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