OCULOSTAT— 510(k) K981235

Substantially Equivalent

Laser Center Dev. Corp.

FDA 510(k) clearance K981235 for OCULOSTAT, Substantially Equivalent on 1998-07-15. Applicant: Laser Center Dev. Corp.. Device class: 1.

Clearance details

Applicant: Laser Center Dev. Corp.
Product code: Code HNC
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1998-04-03
Decision date: 1998-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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