STERI-VERS— 510(k) K810311

Substantially Equivalent

The Hilrad Co.

FDA 510(k) clearance K810311 for STERI-VERS, Substantially Equivalent on 1981-04-17. Applicant: The Hilrad Co.. Device class: 2.

Clearance details

Applicant
The Hilrad Co.
Product code
Code LDS
Device class
Class 2
Regulation
21 CFR 880.6991
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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