FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AIROX AXR. 1A
K Number: K901953
·
Decision Jan 2, 1991
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
57
Review Days
246
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Basic Information
- Device Name
- AIROX AXR. 1A
- K Number
- K901953
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5895
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Ferguson Medical
- Date Received
- May 1, 1990
- Decision Date
- January 2, 1991
- Product Code
- CBK
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | FDA class 2 | Anesthesiology |
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| K Number | Device Name | ||
|---|---|---|---|
| K033153 | DICOM THEATER | Apr 23, 2004 | Substantially Equivalent |
| K963794 | PUNCTURENEEDLE | Mar 19, 1998 | Substantially Equivalent |
| K962615 | TUMORLOCALIZER MRI | Mar 19, 1998 | Substantially Equivalent |
| K971813 | EMBLA | Jan 16, 1998 | Substantially Equivalent |
| K972217 | ORTHOPEDIC SCREW SYSTEM | Nov 20, 1997 | Substantially Equivalent |
| K972219 | ORTHOPEDIC PLATE SYSTEM | Nov 20, 1997 | Substantially Equivalent |
| K970819 | TARGOBEAM | Jul 14, 1997 | Substantially Equivalent |
| K970280 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF PER-TROCHANTEROAM FRACTURES | May 22, 1997 | Substantially Equivalent |
| K970258 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHSIS OF UNSTABLE FEMORAL NECK FRACTURES | May 22, 1997 | Substantially Equivalent |
| K970257 | FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHESIS OF SUB-TROCHANTERIAN FRACTURES | May 22, 1997 | Substantially Equivalent |