510(k) K790689

REVISED BATTERY CHARGER by Vickers America Medical Corp. — Product Code FPL

K790689 is an FDA 510(k) premarket notification submitted by Vickers America Medical Corp. for the device "REVISED BATTERY CHARGER". The FDA issued a decision of Substantially Equivalent on May 29, 1979. The device falls under product code FPL (Incubator, Neonatal Transport), a Class II device regulated under 21 CFR 880.5410. Vickers America Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 29, 1979
Date Received
April 10, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Incubator, Neonatal Transport
Device Class
Class II
Regulation Number
880.5410
Review Panel
HO
Submission Type