MODIFIED SPIROSCAN 1000— 510(k) K897094

Substantially Equivalent

Fukuda Denshi USA, Inc.

FDA 510(k) clearance K897094 for MODIFIED SPIROSCAN 1000, Substantially Equivalent on 1990-01-12. Applicant: Fukuda Denshi USA, Inc..

Clearance details

Applicant: Fukuda Denshi USA, Inc.
Product code: Code BZG
Advisory panel: Anesthesiology
Date received: 1989-12-20
Decision date: 1990-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, WA, US

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