FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PRESSURE INFUSER

K Number: K913751 · Decision Jan 9, 1992
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
35
Applicant Total
10
Review Days
141

Basic Information

Device Name
PRESSURE INFUSER
K Number
K913751
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5420
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BIOMEDICAL DYNAMICS, INC.
Date Received
August 21, 1991
Decision Date
January 9, 1992
Product Code
KZD
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
KZD Infusor, Pressure, For I.V. Bags

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KZD), ordered by most recent decision date.

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Other Clearances by BIOMEDICAL DYNAMICS, INC.

K Number Device Name
K915074 IRRIGATOR/ASPIRATOR PROBE
K911213 CUFFABLE
K911216 INFUSABLE
K911324 IRRIGATION/ASPIRATION TUBING SET
K904376 ANEROID BLOOD PRESSURE GAUGE
K890268 PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION
K881799 BLOOD PRESSURE CUFF
K861977 BIOMEDICAL DYNAMICS DISPOSABLE PRESSURE INFUSOR
K850506 CORRECT FLO INTRAVASCULAR ADMINISTRATION SET