AESCULAP XENON LIGHT SOURCE— 510(k) K984124
Substantially EquivalentAesculap, Inc.
FDA 510(k) clearance K984124 for AESCULAP XENON LIGHT SOURCE, Substantially Equivalent on 1999-02-01. Applicant: Aesculap, Inc.. Device class: 2.
Clearance details
- Applicant
- Aesculap, Inc.
- Product code
- Code FSS
- Device class
- Class 2
- Regulation
- 21 CFR 878.4580
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- South San Francisco, CA, US
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More clearances from Aesculap, Inc.
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