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

PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION

K Number: K890268 · Decision May 5, 1989
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
10
Review Days
107

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION
K Number
K890268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Biomedical Dynamics, Inc.
Date Received
January 18, 1989
Decision Date
May 5, 1989
Product Code
KPE
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
KPE Container, I.V.

Similar 510(k) Clearances

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

View all

Other Clearances by Biomedical Dynamics, Inc.

K Number Device Name
K915074 IRRIGATOR/ASPIRATOR PROBE
K913751 PRESSURE INFUSER
K911213 CUFFABLE
K911216 INFUSABLE
K911324 IRRIGATION/ASPIRATION TUBING SET
K904376 ANEROID BLOOD PRESSURE GAUGE
K881799 BLOOD PRESSURE CUFF
K861977 BIOMEDICAL DYNAMICS DISPOSABLE PRESSURE INFUSOR
K850506 CORRECT FLO INTRAVASCULAR ADMINISTRATION SET