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 | Device Class | Medical Specialty |
|---|---|---|---|
| BRZ | Set, Blood Transfusion | FDA class 2 | General Hospital |
Similar 510(k) Clearances
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PENTATRASFU BLOOD TRANSFUSION SETS
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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 | Dec 17, 1997 | Substantially Equivalent |
| K972839 | PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SET | Dec 17, 1997 | Substantially Equivalent |
| K892623 | PATIENT EXAMINATION GLOVES (LATEX) | Sep 11, 1989 | Substantially Equivalent |
| K884622 | SURGICAL GLOVES | Mar 14, 1989 | Substantially Equivalent |