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

INFANT INCUBATOR

K Number: K780472 · Decision Apr 19, 1978
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
84
Applicant Total
33
Review Days
26

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
INFANT INCUBATOR
K Number
K780472
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Air-Shields, Inc.
Date Received
March 24, 1978
Decision Date
April 19, 1978
Product Code
FMZ
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
FMZ Incubator, Neonatal

Similar 510(k) Clearances

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

View all

Other Clearances by Air-Shields, Inc.

K Number Device Name
K974248 WATCHCHILD OBSTERICAL PATIENT DATA MANAGEMENT SYSTEM
K972309 JM-102 JAUNDICE METER
K971256 DUO-LITE PHOTOTHERAPY SYSTEM
K960980 ISOLETTE INFANT INCUBATOR
K924709 SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETE
K940951 RW RESUCITAIRE INFANT RADIANT WARMER
K940975 C450/C400 INFANT INCUBATORS
K941106 MODEL TI500 ISOLETTE INFANT INCUBATOR
K924170 ISOLETTE INCUBATOR HUMIDITY METER
K922150 EXAMINATION LAMP
Search all 33 clearances from Air-Shields, Inc. →