Atlas FDA

HUMIDIFIER, ELECTRONIC (EH147)

FDA 510(k) clearance K760341 · decided 1976-08-11

Clearance details

K-number
K760341
Device name
HUMIDIFIER, ELECTRONIC (EH147)
Applicant
Mistogen Equipment Co.
Decision
Substantially Equivalent
Date received
1976-07-30
Decision date
1976-08-11
Days to decision
12 days
Clearance type
Traditional
Product code
KFZ
Device class
1
Regulation number
868.5460
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Mistogen Equipment Co.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
THERASTEAM PERSONAL STEAM INHALER (K950116)Kaz, Inc.1995-02-10
VIROTHERM HUMIDIFIER (K915603)Virotherm Laboratory1992-10-22
RHINOTHERM ULTRA 2 (K894734)Twinmed Products, Inc.1990-02-16
WH150 ROOM HUMIDIFIER (K871661)Associated Mills, Inc.1987-06-15
SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 1380 (K871189)Sunbeam Appliance Service Co.1987-05-08
TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER (K862919)Transpirator Technologics, Inc.1986-11-07
MP-500 ELECTRONIC NEBULIZER (K862171)The Timeter Group1986-07-14
SH20, SH30 & SH50 ULTRASONIC HUMIDIFIER (K862042)Associated Mills, Inc.1986-06-05
SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664 (K851220)Northern Electric Co. Div. of Sunbeam Corp.1985-09-17
THERMIX INC. NASOTHERM II PERSONAL STEAM MACHINE (K852283)Thermix, Inc.1985-07-30
INHALATION THERAPY NEBULIZER DEVICE (K850711)Med USA1985-06-05
ULTRASONIC COOL SPRAY HUMIDIFIER (K842275)Sunbeam Corp.1984-08-14

Recalls involving this device

No recalls on record reference this clearance.