510(k) K810792

NEOCARE TEMPERATURE MONITOR by Vickers America Medical Corp. — Product Code FMZ

K810792 is an FDA 510(k) premarket notification submitted by Vickers America Medical Corp. for the device "NEOCARE TEMPERATURE MONITOR". The FDA issued a decision of Substantially Equivalent on April 29, 1981. The device falls under product code FMZ (Incubator, Neonatal), a Class II device regulated under 21 CFR 880.5400. Vickers America Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1981
Date Received
March 23, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Incubator, Neonatal
Device Class
Class II
Regulation Number
880.5400
Review Panel
HO
Submission Type