FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
Atlan
K Number: K230931
·
Decision Jul 23, 2023
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
2
Review Days
111
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Basic Information
- Device Name
- Atlan
- K Number
- K230931
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5160
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Drägerwerk AG Co. Kgaa
- Date Received
- April 3, 2023
- Decision Date
- July 23, 2023
- 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 |
Similar 510(k) Clearances
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Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)
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Other Clearances by Drägerwerk AG Co. Kgaa
| K Number | Device Name | ||
|---|---|---|---|
| K252746 | Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) | May 21, 2026 | Substantially Equivalent |