CLINICAL ANALYZER SYSTEM— 510(k) K780903
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K780903 for CLINICAL ANALYZER SYSTEM, Substantially Equivalent on 1978-06-28. Applicant: Bausch & Lomb, Inc.. Device class: 1.
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code JJQ
- Device class
- Class 1
- Regulation
- 21 CFR 862.2300
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.