510(k) K861977

BIOMEDICAL DYNAMICS DISPOSABLE PRESSURE INFUSOR by Biomedical Dynamics, Inc. — Product Code KZD

K861977 is an FDA 510(k) premarket notification submitted by Biomedical Dynamics, Inc. for the device "BIOMEDICAL DYNAMICS DISPOSABLE PRESSURE INFUSOR". The FDA issued a decision of Substantially Equivalent on July 15, 1986. The device falls under product code KZD (Infusor, Pressure, For I.V. Bags), a Class I device regulated under 21 CFR 880.5420. Biomedical Dynamics, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 15, 1986
Date Received
May 21, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Infusor, Pressure, For I.V. Bags
Device Class
Class I
Regulation Number
880.5420
Review Panel
HO
Submission Type