FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
ATA HCM MONOPLACE HYPERBARIC SYSTEM
K Number: K040145
·
Decision May 4, 2005
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
68
Applicant Total
1
Review Days
468
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Basic Information
- Device Name
- ATA HCM MONOPLACE HYPERBARIC SYSTEM
- K Number
- K040145
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5470
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Ata Hyperbaric Chamber Manufacturing
- Date Received
- January 22, 2004
- Decision Date
- May 4, 2005
- Product Code
- CBF
- 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 |
|---|---|---|---|
| CBF | Chamber, Hyperbaric | FDA class 2 | Anesthesiology |
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