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

PALL EC PLUS FILTER W/FILTER SLEEVE

K Number: K834382 · Decision Aug 3, 1984
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
28
Review Days
233

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Basic Information

Device Name
PALL EC PLUS FILTER W/FILTER SLEEVE
K Number
K834382
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pall Biomedical Products Co.
Date Received
December 14, 1983
Decision Date
August 3, 1984
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

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Other Clearances by Pall Biomedical Products Co.

K Number Device Name
K954331 PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER)
K960993 PALL SQ40S BLOOD FILTER (SQ40S/SQ40ST)
K905794 PALL 3N1 FILTER
K902518 LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE
K884534 PALL HEPCHEK (TM) HEPARIN ABSORPTION FILTER
K875095 PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE
K875094 ULTIPOR PRE-BYPASS PLUS FILTER W/POSIDYNE MEMBRANE
K873667 PALL LEUKOCYTE REMOVAL FILTER, PLATELETS
K873666 PALL LEUKOCYTE REMOVAL FILTER, BLOOD
K874405 PALL STAT PRIME(TM) BLOOD FILTER FOR EXTRA. USE
Search all 28 clearances from Pall Biomedical Products Co. →