510(k) K844879

HUNTLEIGH ALPHACARE, HM95 ALTERNATING PRESS-PUMP by Huntleigh Technology, Inc. — Product Code FNM

K844879 is an FDA 510(k) premarket notification submitted by Huntleigh Technology, Inc. for the device "HUNTLEIGH ALPHACARE, HM95 ALTERNATING PRESS-PUMP". The FDA issued a decision of Substantially Equivalent on January 25, 1985. The device falls under product code FNM (Mattress, Air Flotation, Alternating Pressure), a Class II device regulated under 21 CFR 880.5550. Huntleigh Technology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 25, 1985
Date Received
December 17, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mattress, Air Flotation, Alternating Pressure
Device Class
Class II
Regulation Number
880.5550
Review Panel
HO
Submission Type