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FDA 510(k)

FPC FECAL PARASITE CONCENTRATOR

K-Number: K833469 · 1983-11-28

Decision Date1983-11-28
Product CodeLKS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FPC FECAL PARASITE CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Evergreen Scientific, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833469. The device is classified under product code LKS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FPC FECAL PARASITE CONCENTRATOR?

FPC FECAL PARASITE CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Evergreen Scientific, Inc.. The 510(k) number is K833469.

When did FPC FECAL PARASITE CONCENTRATOR receive FDA 510(k) clearance?

FPC FECAL PARASITE CONCENTRATOR received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833469.

Who is the listed applicant for FPC FECAL PARASITE CONCENTRATOR?

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

What is the FDA product code for FPC FECAL PARASITE CONCENTRATOR?

The FDA product code for FPC FECAL PARASITE CONCENTRATOR is LKS.

Related Clinical Trials

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.

Other records listing Evergreen Scientific, Inc. 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.

Related Devices (Code: LKS)

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.

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.

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