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

L-3 PURGE LINE

K Number: K802602 · Decision Nov 12, 1980
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
27
Review Days
22

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Basic Information

Device Name
L-3 PURGE LINE
K Number
K802602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Delta Medical Industries
Date Received
October 21, 1980
Decision Date
November 12, 1980
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 Delta Medical Industries

K Number Device Name
K833884 ISOTEC DISPOS. PRESSURE TRANSDUCER
K840253 ONE-WAY AIR VALVE
K832470 INFUSION PUMP
K830389 ACCU-RYNGE PUMP SP-250
K831750 PM-3
K822761 DELIVERY TUBE SET #2226
K820912 PMS-2 PRESSURE MONITOR SEPARATOR
K820482 ACCU-RYNGE INSULIN PUMP #SP-250
K810068 PEDIATRIC ARTERIAL BLOOD FILTER
K802755 ARTERIAL BLOOD FILTER BF-37
Search all 27 clearances from Delta Medical Industries →