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

FLUSH DEVICE, AUTOMATIC

K Number: K851987 · Decision Aug 16, 1985
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
147
Applicant Total
7
Review Days
101

Basic Information

Device Name
FLUSH DEVICE, AUTOMATIC
K Number
K851987
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2850
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
TRANSAMERICA DELAVAL, INC.
Date Received
May 7, 1985
Decision Date
August 16, 1985
Product Code
DRS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DRS Transducer, Blood-Pressure, Extravascular

Similar 510(k) Clearances

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

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Other Clearances by TRANSAMERICA DELAVAL, INC.

K Number Device Name
K853996 DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE
K851989 DOME, DISPOSABLE, STERILE
K851988 ADMINISTRATION SET
K851986 STOPCOCKS
K833171 MONITORING KIT
K833170 FLUSH DEVICE