ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202— 510(k) K800364

Substantially Equivalent

Hoffrel Instruments, Inc.

FDA 510(k) clearance K800364 for ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202, Substantially Equivalent on 1980-03-12. Applicant: Hoffrel Instruments, Inc..

Clearance details

Applicant: Hoffrel Instruments, Inc.
Product code: Code DKX
Advisory panel: Clinical Toxicology
Date received: 1980-02-20
Decision date: 1980-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.