FDA 510(k)

PHYTOHAEMAGGLUTININ

K-Number: K790239 · 1979-03-08

Decision Date1979-03-08

Product CodeKIQ

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

PHYTOHAEMAGGLUTININ is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Fine Chemicals. It received FDA 510(k) clearance on 1979-03-08 under 510(k) number K790239. The device is classified under product code KIQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYTOHAEMAGGLUTININ?

PHYTOHAEMAGGLUTININ is a medical device that received FDA 510(k) clearance on 1979-03-08. The listed applicant is Pharmacia Fine Chemicals. The 510(k) number is K790239.

When did PHYTOHAEMAGGLUTININ receive FDA 510(k) clearance?

PHYTOHAEMAGGLUTININ received FDA 510(k) clearance on 1979-03-08, under 510(k) number K790239.

Who is the listed applicant for PHYTOHAEMAGGLUTININ?

The FDA 510(k) record lists Pharmacia Fine Chemicals as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHYTOHAEMAGGLUTININ?

The FDA product code for PHYTOHAEMAGGLUTININ is KIQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.