FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇷 Argentina

MEDIX PC-305 NEONATAL INCUBATOR

K Number: K920049 · Decision May 21, 1993
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
84
Applicant Total
6
Review Days
501

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
MEDIX PC-305 NEONATAL INCUBATOR
K Number
K920049
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medix I.C.S.A.
Date Received
January 6, 1992
Decision Date
May 21, 1993
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 Medix I.C.S.A.

K Number Device Name
K103735 MEDILED MINI
K083179 MEDILED PHOTOTHERAPY LAMP
K070291 MEDIX NATAL CARE INTENSIVE CARE INCUBATOR, MODELS-NATAL CARE ST-MX/LX/BX
K931529 INFANT WARMER
K931965 MEDIX PHOTOTHERAPY LAMP