REFRACTEC MCS-100— 510(k) K980522

Unknown

Refractec, Inc.

FDA 510(k) clearance K980522 for REFRACTEC MCS-100, Unknown on 1998-07-22. Applicant: Refractec, Inc.. Device class: 2.

Clearance details

Applicant: Refractec, Inc.
Product code: Code HQR
Device class: Class 2
Regulation: 21 CFR 886.4100
Advisory panel: Ophthalmic
Date received: 1998-02-10
Decision date: 1998-07-22
Decision: Unknown
Clearance type: Traditional
Location: Laguna Hills, CA, US

Download summary PDF View on FDA.gov ↗

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