AESCULAP PNEUMATIC KERRISON— 510(k) K062413
Substantially EquivalentAesculap, Inc.
FDA 510(k) clearance K062413 for AESCULAP PNEUMATIC KERRISON, Substantially Equivalent on 2006-11-21. Applicant: Aesculap, Inc.. Device class: 2.
Clearance details
- Applicant
- Aesculap, Inc.
- Product code
- Code HAD
- Device class
- Class 2
- Regulation
- 21 CFR 882.4845
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Center Valley, PA, US
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