FDA 510(k)

CLINETICS PCA COLUMN

K-Number: K801306 · 1980-09-26

Decision Date1980-09-26

Product CodeDHX

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

CLINETICS PCA COLUMN is the device name listed in this FDA 510(k) record. The listed applicant is Clinetics Corp.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801306. The device is classified under product code DHX. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINETICS PCA COLUMN?

CLINETICS PCA COLUMN is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Clinetics Corp.. The 510(k) number is K801306.

When did CLINETICS PCA COLUMN receive FDA 510(k) clearance?

CLINETICS PCA COLUMN received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801306.

Who is the listed applicant for CLINETICS PCA COLUMN?

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

What is the FDA product code for CLINETICS PCA COLUMN?

The FDA product code for CLINETICS PCA COLUMN is DHX.

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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.