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

Panda iRes Warmer, Giraffe Warmer

K Number: K201628 · Decision Feb 12, 2021
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
91
Applicant Total
168
Review Days
241

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
Panda iRes Warmer, Giraffe Warmer
K Number
K201628
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
June 16, 2020
Decision Date
February 12, 2021
Product Code
FMT
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
FMT Warmer, Infant Radiant

Similar 510(k) Clearances

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

View all

Other Clearances by GE Healthcare

K Number Device Name
K253639 View
K242925 MR Contour DL
K232346 Digital Expert Access with Remote Scanning
K223212 Precision DL
K221680 Xeleris V Processing and Review System
K221932 Omni Legend
K213689 Voluson P6, Voluson P8
K213642 Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert
K211488 LOGIQ E10
K211524 LOGIQ E10s, LOGIQ Fortis
Search all 168 clearances from GE Healthcare →