510(k) K813239

OXYGENAIRE NURING INCUBATOR by Vickers America Medical Corp. — Product Code FMZ

K813239 is an FDA 510(k) premarket notification submitted by Vickers America Medical Corp. for the device "OXYGENAIRE NURING INCUBATOR". The FDA issued a decision of Substantially Equivalent on January 28, 1982. 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
January 28, 1982
Date Received
November 17, 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