Microlab 4000, Microlab 4200

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K961896 ↗

FDA Product Code

JQW

Device Class

Class I

Regulation

21 CFR Part 862.2750

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Discrete Photometric Chemistry Analyzer

  Class I

  FDA 510(k) K943493 Active Cleared 30 Jan 1995

• Microlab P

  Class I

  FDA 510(k) K832204 Active Cleared 24 Aug 1983

• Pb 600 Repeating Dispenser

  Class I

  FDA 510(k) K832202 Active Cleared 24 Aug 1983

• Multi-Probe Head Plus

  Class I

  FDA 510(k) K892369 Active Cleared 2 Jun 1989

• Precision Liquid Dispenser

  Class I

  FDA 510(k) K832205 Active Cleared 24 Aug 1983

• Chrom-Prep

  Class I

  FDA 510(k) K832201 Active Cleared 16 Aug 1983

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