LINDQUIST MODEL 370— 510(k) K893980
Substantially EquivalentR.J. Lindquist Co.
FDA 510(k) clearance K893980 for LINDQUIST MODEL 370, Substantially Equivalent on 1990-08-02. Applicant: R.J. Lindquist Co.. Device class: 2.
Clearance details
- Applicant
- R.J. Lindquist Co.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
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