PROFESSIONAL MONITOR— 510(k) K901907

Substantially Equivalent

Travis Industries, Inc.

FDA 510(k) clearance K901907 for PROFESSIONAL MONITOR, Substantially Equivalent on 1990-09-12. Applicant: Travis Industries, Inc.. Device class: 2.

Clearance details

Applicant: Travis Industries, Inc.
Product code: Code KPN
Device class: Class 2
Regulation: 21 CFR 876.2040
Advisory panel: Gastroenterology, Urology
Date received: 1990-04-27
Decision date: 1990-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Coos Bay, OR, US

Download summary PDF View on FDA.gov ↗

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More clearances from Travis Industries, Inc.

K903856 — WET-NO-MORE MONITOR1990-09-12
K901906 — WET-NO-MORE MONITOR1990-07-11

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