L SOPHIA— 510(k) K901512

Substantially Equivalent

Nishitomo Co., Inc.

FDA 510(k) clearance K901512 for L SOPHIA, Substantially Equivalent on 1990-07-20. Applicant: Nishitomo Co., Inc.. Device class: Unclassified.

Clearance details

Applicant: Nishitomo Co., Inc.
Product code: Code LHD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1990-03-29
Decision date: 1990-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Japan, JP

Download summary PDF View on FDA.gov ↗

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