HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODY— 510(k) K962730
Substantially EquivalentHycor Biomedical, Inc.
FDA 510(k) clearance K962730 for HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODY, Substantially Equivalent on 1997-03-07. Applicant: Hycor Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Hycor Biomedical, Inc.
- Product code
- Code LRM
- Device class
- Class 2
- Regulation
- 21 CFR 866.5100
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Garden Grove, CA, US
Recent devices under product code LRM
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