FDA 510(k)

CLINICAL ACQUISITION MODULE

K-Number: K780971 · 1978-06-22

ApplicantAnalytical Development Assoc. Corp.

Decision Date1978-06-22

Product CodeIYX

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CLINICAL ACQUISITION MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Development Assoc. Corp.. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780971. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL ACQUISITION MODULE?

CLINICAL ACQUISITION MODULE is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Analytical Development Assoc. Corp.. The 510(k) number is K780971.

When did CLINICAL ACQUISITION MODULE receive FDA 510(k) clearance?

CLINICAL ACQUISITION MODULE received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780971.

Who is the listed applicant for CLINICAL ACQUISITION MODULE?

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

What is the FDA product code for CLINICAL ACQUISITION MODULE?

The FDA product code for CLINICAL ACQUISITION MODULE is IYX.

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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.