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FDA 510(k)

AKERSCAN COLORIMETRIC ANALYZER

K-Number: K862908 · 1986-09-15

ApplicantAkers Medical Technologies
Decision Date1986-09-15
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AKERSCAN COLORIMETRIC ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Akers Medical Technologies. It received FDA 510(k) clearance on 1986-09-15 under 510(k) number K862908. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKERSCAN COLORIMETRIC ANALYZER?

AKERSCAN COLORIMETRIC ANALYZER is a medical device that received FDA 510(k) clearance on 1986-09-15. The listed applicant is Akers Medical Technologies. The 510(k) number is K862908.

When did AKERSCAN COLORIMETRIC ANALYZER receive FDA 510(k) clearance?

AKERSCAN COLORIMETRIC ANALYZER received FDA 510(k) clearance on 1986-09-15, under 510(k) number K862908.

Who is the listed applicant for AKERSCAN COLORIMETRIC ANALYZER?

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

What is the FDA product code for AKERSCAN COLORIMETRIC ANALYZER?

The FDA product code for AKERSCAN COLORIMETRIC ANALYZER is JJQ.

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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.

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