PLT-4 Platelet Analyzer

FDA 510(k) K853722 · Texas Intl. Laboratories, Inc.

Substantially Equivalent

510(k) numberK853722

Submission

Device name
PLT-4 Platelet Analyzer
Applicant
Texas Intl. Laboratories, Inc.
Houston, TX, US
Received
September 5, 1985
Decision date
January 17, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKL – Counter, Cell, Automated (Particle Counter)
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5200
Specialty
Hematology

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K884006Hemat 12GKZ · Traditional 12/05/1988SE
K883177H 10 or Hematil 10 Blood Cell & Platelet CounterGKZ · Traditional 11/30/1988SE
K832886Flame Photometer T281-T282-T283JJO · Traditional 12/08/1983SE
K832890Hemacomp 7 or Hematil 7GKL · Traditional 10/19/1983SE
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Questions and answers

When was PLT-4 Platelet Analyzer cleared by the FDA?

PLT-4 Platelet Analyzer (K853722) received a 510(k) decision of Substantially Equivalent on January 17, 1986, 134 days after the submission was received.

What is the product code of K853722?

The FDA product code is GKL – Counter, Cell, Automated (Particle Counter), a Class II (moderate risk) device regulated under 21 CFR 864.5200.