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

FILTER, ARTERIAL BLOOD W/TUBING BYPASS

K Number: K781707 · Decision Oct 26, 1978
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
56
Review Days
16

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Basic Information

Device Name
FILTER, ARTERIAL BLOOD W/TUBING BYPASS
K Number
K781707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Surgikos, Inc.
Date Received
October 10, 1978
Decision Date
October 26, 1978
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 Surgikos, Inc.

K Number Device Name
K875107 HEALTH CARE EYE PROTECTION
K874653 STERILE SURGICAL SCRUB BRUSH
K861441 NEUTRALON SURGICAL GLOVES
K852870 BARRIER SURGICAL GOWN
K822535 CIDEX*DIALYZER DISINFECTING SOLUTION
K820543 BARRIER ANTIMICROBIAL INCISE DRAPE
K820542 SURGIKOS INCISE DRAPE
K811871 BACTERICIDAL INCISE DRAPE
K810316 SURGIKOS FACE MASK
K801864 BARRIER APERTURED DRAPE
Search all 56 clearances from Surgikos, Inc. →