STERILIZATION INDICATOR/SEAL PROTECTOR— 510(k) K811408

Name: FDA 510(k) clearance K811408
Creator: U.S. Food and Drug Administration
Published: 1981-06-12

Substantially Equivalent

Beacon Converters, Inc.

FDA 510(k) clearance K811408 for STERILIZATION INDICATOR/SEAL PROTECTOR, Substantially Equivalent on 1981-06-12. Applicant: Beacon Converters, Inc.. Device class: 2.

Clearance details

Applicant: Beacon Converters, Inc.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1981-05-19
Decision date: 1981-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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