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

IMPRAFLO POSTOPERATIVE AUTOTRANSFUSION DEVICE

K Number: K915577 · Decision Mar 11, 1992
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
29
Review Days
89

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Basic Information

Device Name
IMPRAFLO POSTOPERATIVE AUTOTRANSFUSION DEVICE
K Number
K915577
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2460
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Impra, Inc.
Date Received
December 13, 1991
Decision Date
March 11, 1992
Product Code
CAR
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
CAR Monitor, Spinal-Fluid Pressure, Electrically Powered

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Other Clearances by Impra, Inc.

K Number Device Name
K004012 IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
K004011 IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS
K991027 BI-DIRECTIONAL TUNNELER
K983769 DISTAFLO BYPASS GRAFT
K983861 DISTAFLO BYPASS GRAFT
K983064 IMPRA HIGH POROSITY GRAFT
K981076 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K981079 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K971192 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964877 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
Search all 29 clearances from Impra, Inc. →