KELLER VITAL SIGNS MONITOR - KMS-890— 510(k) K910262

Name: FDA 510(k) clearance K910262
Creator: U.S. Food and Drug Administration
Published: 1991-04-01

Substantially Equivalent

Keller Medical Specialties Products, Inc.

FDA 510(k) clearance K910262 for KELLER VITAL SIGNS MONITOR - KMS-890, Substantially Equivalent on 1991-04-01. Applicant: Keller Medical Specialties Products, Inc.. Device class: 2.

Clearance details

Applicant: Keller Medical Specialties Products, Inc.
Product code: Code DSJ
Device class: Class 2
Regulation: 21 CFR 870.1100
Advisory panel: Cardiovascular
Date received: 1991-01-22
Decision date: 1991-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Antioch, IL, US

Download summary PDF View on FDA.gov ↗

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