THE KEYMED FIBERSCOPE STERILIZATION CASE— 510(k) K860528

Name: FDA 510(k) clearance K860528
Creator: U.S. Food and Drug Administration
Published: 1986-07-15

Substantially Equivalent

Keymed, Inc.

FDA 510(k) clearance K860528 for THE KEYMED FIBERSCOPE STERILIZATION CASE, Substantially Equivalent on 1986-07-15. Applicant: Keymed, Inc.. Device class: 2.

Clearance details

Applicant: Keymed, Inc.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 1986-02-11
Decision date: 1986-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Essex Ss2 5qh England, GB

Download summary PDF View on FDA.gov ↗

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