FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER

K Number: K862042 · Decision Jun 5, 1986
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
19
Applicant Total
14
Review Days
8

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
SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER
K Number
K862042
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5460
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Associated Mills, Inc.
Date Received
May 28, 1986
Decision Date
June 5, 1986
Product Code
KFZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

Similar 510(k) Clearances

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

View all

Other Clearances by Associated Mills, Inc.

K Number Device Name
K901459 DS60 TOOTHBRUSH SANITIZER
K872327 WHIRLPOOL AERATOR WB700, WB800, WB900, WB975
K871661 WH150 ROOM HUMIDIFIER
K862041 WM10, WM20, WM30 POWER MASSAGER
K844396 POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000
K844397 POLLENEX DIGITAL SPHYGMOMANOMETER BP-4000
K850363 POLLENEX DIGITAL THERMOMETER T-225
K850362 POLLENEX DIGITAL THERMOMETER T-125
K841095 BP800, 850 1000
K841100 HP-20, 30, 40, 50 & 60
Search all 14 clearances from Associated Mills, Inc. →