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

PROTOS BLOOD TRANSFUSION SET

K Number: K972843 · Decision Dec 16, 1997
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
29
Applicant Total
5
Review Days
137

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Basic Information

Device Name
PROTOS BLOOD TRANSFUSION SET
K Number
K972843
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Globe Ent., Inc.
Date Received
August 1, 1997
Decision Date
December 16, 1997
Product Code
BRZ
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
BRZ Set, Blood Transfusion

Similar 510(k) Clearances

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

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Other Clearances by Globe Ent., Inc.

K Number Device Name
K972854 PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARY
K972839 PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SET
K892623 PATIENT EXAMINATION GLOVES (LATEX)
K884622 SURGICAL GLOVES