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PHYTOHAEMAGGLUTININ

K790239 Class I Traditional
Decision Date
1979-03-08
Sponsor / Applicant
Pharmacia Fine Chemicals

Technical Specification

510(k) Submission ID K790239
Product Code KIQ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.2260
Decision Date 1979-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHYTOHAEMAGGLUTININ received FDA 510(k) clearance under submission number K790239, sponsored by Pharmacia Fine Chemicals. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1979-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code KIQ and 21 CFR 864.2260, within the Hematology review panel as a Class I device.