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

AERO PULSE ALTERNATING PRES. PUMP

K Number: K771463 · Decision Aug 26, 1977
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
101
Applicant Total
165
Review Days
22

Basic Information

Device Name
AERO PULSE ALTERNATING PRES. PUMP
K Number
K771463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
MEDLINE INDUSTRIES, INC.
Date Received
August 4, 1977
Decision Date
August 26, 1977
Product Code
FNM
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
FNM Mattress, Air Flotation, Alternating Pressure

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