Microlab P

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

510(k) Number

K832204 ↗

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

• 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

• Digital Diluter/Dispensers

  Class I

  FDA 510(k) K822688 Active Cleared 5 Nov 1982

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