REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801— 510(k) K873832
Substantially EquivalentIn Vitro Diagnostics, Inc.
FDA 510(k) clearance K873832 for REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801, Substantially Equivalent on 1987-11-23. Applicant: In Vitro Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- In Vitro Diagnostics, Inc.
- Product code
- Code KRZ
- Device class
- Class 2
- Regulation
- 21 CFR 864.8165
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
Recent devices under product code KRZ
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