G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8— 510(k) K071132
Substantially EquivalentTosoh Bioscience, Inc.
FDA 510(k) clearance K071132 for G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8, Substantially Equivalent on 2008-09-16. Applicant: Tosoh Bioscience, Inc.. Device class: 2.
Clearance details
- Applicant
- Tosoh Bioscience, Inc.
- Product code
- Code LCP
- Device class
- Class 2
- Regulation
- 21 CFR 864.7470
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- South San Franciso, CA, US
Recent devices under product code LCP
view allMore clearances from Tosoh Bioscience, Inc.
view allRecalls naming K071132
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 K071132.
Data sourced from openFDA. This site is unofficial and independent of the FDA.