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FDA 510(k)

PROACTIVATOR C3, C4 AND C3

K-Number: K790059 · 1979-03-15

ApplicantIcl Scientific
Decision Date1979-03-15
Product CodeKTP
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

PROACTIVATOR C3, C4 AND C3 is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1979-03-15 under 510(k) number K790059. The device is classified under product code KTP. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROACTIVATOR C3, C4 AND C3?

PROACTIVATOR C3, C4 AND C3 is a medical device that received FDA 510(k) clearance on 1979-03-15. The listed applicant is Icl Scientific. The 510(k) number is K790059.

When did PROACTIVATOR C3, C4 AND C3 receive FDA 510(k) clearance?

PROACTIVATOR C3, C4 AND C3 received FDA 510(k) clearance on 1979-03-15, under 510(k) number K790059.

Who is the listed applicant for PROACTIVATOR C3, C4 AND C3?

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

What is the FDA product code for PROACTIVATOR C3, C4 AND C3?

The FDA product code for PROACTIVATOR C3, C4 AND C3 is KTP.

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Other records listing Icl Scientific as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

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

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