STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)— 510(k) K952151

Name: FDA 510(k) clearance K952151
Creator: U.S. Food and Drug Administration
Published: 1996-03-04

Substantially Equivalent

Storz

FDA 510(k) clearance K952151 for STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204), Substantially Equivalent on 1996-03-04. Applicant: Storz. Device class: 2.

Clearance details

Applicant: Storz
Product code: Code HQR
Device class: Class 2
Regulation: 21 CFR 886.4100
Advisory panel: Ophthalmic
Date received: 1995-05-08
Decision date: 1996-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQR

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K955158 — SURGITRON1996-02-09

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K926512 — STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE1993-09-09
K913504 — STORZ MICRO CUTTER 25 GAUGE PACK1992-02-21

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