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

TEMPROBE MONITOR

K Number: K840648 · Decision Jun 5, 1984
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
75
Review Days
111

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TEMPROBE MONITOR
K Number
K840648
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Vital Signs, Inc.
Date Received
February 15, 1984
Decision Date
June 5, 1984
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLL), ordered by most recent decision date.

View all

Other Clearances by Vital Signs, Inc.

K Number Device Name
K112902 ENFLOW IV FLUID WARMER
K041309 IMASK TM
K030985 BREAS PV 10I CPAP SYSTEM, MODEL PV 10I
K022402 DISPOSABLE PRESSURE MANOMETER
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
Search all 75 clearances from Vital Signs, Inc. →