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FDA 510(k)

FORMA-FAS-TEST

K-Number: K833128 · 1984-06-27

ApplicantChemical Detection & Experimentation
Decision Date1984-06-27
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FORMA-FAS-TEST is the device name listed in this FDA 510(k) record. The listed applicant is Chemical Detection & Experimentation. It received FDA 510(k) clearance on 1984-06-27 under 510(k) number K833128. The device is classified under product code LIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORMA-FAS-TEST?

FORMA-FAS-TEST is a medical device that received FDA 510(k) clearance on 1984-06-27. The listed applicant is Chemical Detection & Experimentation. The 510(k) number is K833128.

When did FORMA-FAS-TEST receive FDA 510(k) clearance?

FORMA-FAS-TEST received FDA 510(k) clearance on 1984-06-27, under 510(k) number K833128.

Who is the listed applicant for FORMA-FAS-TEST?

The FDA 510(k) record lists Chemical Detection & Experimentation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORMA-FAS-TEST?

The FDA product code for FORMA-FAS-TEST is LIF.

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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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