CASPAR SCALP CLIP, APPLIER— 510(k) K890443
Substantially EquivalentAesculap Instruments Corp.
FDA 510(k) clearance K890443 for CASPAR SCALP CLIP, APPLIER, Substantially Equivalent on 1989-06-15. Applicant: Aesculap Instruments Corp.. Device class: 2.
Clearance details
- Applicant
- Aesculap Instruments Corp.
- Product code
- Code HBO
- Device class
- Class 2
- Regulation
- 21 CFR 882.4150
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Burlingame, CA, US
Recent devices under product code HBO
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