KARICKHOFF FLYING CORPUSCLE VIEWER— 510(k) K831829

Name: FDA 510(k) clearance K831829
Creator: U.S. Food and Drug Administration
Published: 1983-10-19

Substantially Equivalent

Surgidev Corp.

FDA 510(k) clearance K831829 for KARICKHOFF FLYING CORPUSCLE VIEWER, Substantially Equivalent on 1983-10-19. Applicant: Surgidev Corp.. Device class: 1.

Clearance details

Applicant: Surgidev Corp.
Product code: Code HIX
Device class: Class 1
Regulation: 21 CFR 886.1435
Advisory panel: Ophthalmic
Date received: 1983-06-07
Decision date: 1983-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIX

view all

K801554 — STERILE CAST PADDING1980-08-04

More clearances from Surgidev Corp.

view all

K850729 — ACUFLO VOLUMETRIC CONTROLLED DELIVERY SYS 20001985-04-09
K831975 — LEADING EDGE OPHTHALMIC KNIFE1983-08-31
K830008 — KARICKHOFF KERATOSCOPE1983-01-26

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