LIQUICHEK TORCH PLUS IGM CONTROL— 510(k) K040822
Substantially EquivalentBio-Rad Laboratories, Inc.
FDA 510(k) clearance K040822 for LIQUICHEK TORCH PLUS IGM CONTROL, Substantially Equivalent on 2004-05-19. Applicant: Bio-Rad Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Bio-Rad Laboratories, Inc.
- Product code
- Code JJY
- Device class
- Class 1
- Regulation
- 21 CFR 862.1660
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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More clearances from Bio-Rad Laboratories, Inc.
view allRecalls naming K040822
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K040822.
Data sourced from openFDA. This site is unofficial and independent of the FDA.