FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Medline Digital Thermometer Non-Lubricated Probe Sheath

K Number: K211931 · Decision Sep 20, 2021
Classifications
1
FEI Numbers
518
Registration Numbers
518
Same Product Code
795
Applicant Total
59
Review Days
90

Basic Information

Device Name
Medline Digital Thermometer Non-Lubricated Probe Sheath
K Number
K211931
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medline Industries, Inc.
Date Received
June 22, 2021
Decision Date
September 20, 2021
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FLL Continuous Measurement Thermometer

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