LD 400— 510(k) K930937

Substantially Equivalent

Vismed, Inc.

FDA 510(k) clearance K930937 for LD 400, Substantially Equivalent on 1993-10-18. Applicant: Vismed, Inc.. Device class: 1.

Clearance details

Applicant: Vismed, Inc.
Product code: Code HPT
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1993-02-23
Decision date: 1993-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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