TYCOS DIAGNOSTIC PENLIGHT— 510(k) K760972

Name: FDA 510(k) clearance K760972
Creator: U.S. Food and Drug Administration
Published: 1977-01-26

Substantially Equivalent

Taylor Instrument Analytics Co.

FDA 510(k) clearance K760972 for TYCOS DIAGNOSTIC PENLIGHT, Substantially Equivalent on 1977-01-26. Applicant: Taylor Instrument Analytics Co.. Device class: 1.

Clearance details

Applicant: Taylor Instrument Analytics Co.
Product code: Code KYT
Device class: Class 1
Regulation: 21 CFR 880.6350
Advisory panel: General Hospital
Date received: 1976-11-04
Decision date: 1977-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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