SONOMICROMETER, ULTRASONIC DIMENSION SYSTEM, CARD.— 510(k) K885349

Name: FDA 510(k) clearance K885349
Creator: U.S. Food and Drug Administration
Published: 1989-06-22

Substantially Equivalent

Sonotek Corp.

FDA 510(k) clearance K885349 for SONOMICROMETER, ULTRASONIC DIMENSION SYSTEM, CARD., Substantially Equivalent on 1989-06-22. Applicant: Sonotek Corp.. Device class: 2.

Clearance details

Applicant: Sonotek Corp.
Product code: Code DXK
Device class: Class 2
Regulation: 21 CFR 870.2330
Advisory panel: Cardiovascular
Date received: 1988-12-28
Decision date: 1989-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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