OPHTHASONIC A/P III— 510(k) K903666

Substantially Equivalent

Teknar, Inc.

FDA 510(k) clearance K903666 for OPHTHASONIC A/P III, Substantially Equivalent on 1990-11-19. Applicant: Teknar, Inc.. Device class: 1.

Clearance details

Applicant: Teknar, Inc.
Product code: Code HPY
Device class: Class 1
Regulation: 21 CFR 886.4250
Advisory panel: Ophthalmic
Date received: 1990-08-14
Decision date: 1990-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fenton, MO, US

Download summary PDF View on FDA.gov ↗

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K891777 — PRO-CUT BIOPSY NEEDLE1989-05-04
K883965 — PROBE, IMAGING, ULTRASONIC, MECHANICAL SECTOR1988-10-05
K881850 — TEKNAR PERCU-SCAN1988-08-29

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