ALIGNMENT INSTRUMENT— 510(k) K970345
Substantially EquivalentRichard Wolf Medical Instruments Corp.
FDA 510(k) clearance K970345 for ALIGNMENT INSTRUMENT, Substantially Equivalent on 1997-04-29. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 1.
Clearance details
- Applicant
- Richard Wolf Medical Instruments Corp.
- Product code
- Code HSZ
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vernon Hills, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.