FDA 510(k)
FDA class 1
Substantially Equivalent
🇦🇺 Australia
NASCOR IGLOO
K Number: K935126
·
Decision Oct 18, 1994
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
10
Applicant Total
2
Review Days
355
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Basic Information
- Device Name
- NASCOR IGLOO
- K Number
- K935126
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5700
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Nascor Pty. , Ltd.
- Date Received
- October 28, 1993
- Decision Date
- October 18, 1994
- Product Code
- BYL
- 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 |
|---|---|---|---|
| BYL | Tent, Oxygen | FDA class 1 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BYL), ordered by most recent decision date.
NASCOR OXYDOME
FDA 510(k)
FDA Class 1
·Anesthesiology
SPAG PAK
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FDA Class 1
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DIRD INGANT O2 (BIO 2 HOOD)
FDA 510(k)
FDA Class 1
·Anesthesiology
NOVA OXYGEN TENT
FDA 510(k)
FDA Class 1
·Anesthesiology
KEYSTONE OXYGEN TENT
FDA 510(k)
FDA Class 1
·Anesthesiology
AEROSOL DELIVERY HOOD
FDA 510(k)
FDA Class 1
·Anesthesiology
Other Clearances by Nascor Pty. , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K905627 | NASCOR OXYDOME | Jun 3, 1991 | Substantially Equivalent |