RK VACUUM FIXATION RING SYSTEM— 510(k) K863775

Substantially Equivalent

Ameritek, Inc.

FDA 510(k) clearance K863775 for RK VACUUM FIXATION RING SYSTEM, Substantially Equivalent on 1986-10-20. Applicant: Ameritek, Inc.. Device class: 1.

Clearance details

Applicant: Ameritek, Inc.
Product code: Code HNH
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1986-09-26
Decision date: 1986-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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