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

PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE

K Number: K980762 · Decision Sep 1, 1998
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
3
Review Days
186

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Basic Information

Device Name
PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE
K Number
K980762
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pall Corp.
Date Received
February 27, 1998
Decision Date
September 1, 1998
Product Code
DTM
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
DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

Similar 510(k) Clearances

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

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Other Clearances by Pall Corp.

K Number Device Name
K022167 PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEM
K993379 PALL SUPOR AEF FILTER