FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PERSEUS A500
K Number: K133886
·
Decision Jun 20, 2014
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
4
Review Days
182
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Basic Information
- Device Name
- PERSEUS A500
- K Number
- K133886
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5160
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Draeger Medical GmbH
- Date Received
- December 20, 2013
- Decision Date
- June 20, 2014
- Product Code
- BSZ
- 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 |
|---|---|---|---|
| BSZ | Gas-Machine, Anesthesia | FDA class 2 | Anesthesiology |
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