FDA 510(k)

DIACYTE FIXATIVE SOLUTION

K-Number: K880549 · 1988-04-01

Decision Date1988-04-01

Product CodeLDY

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

DIACYTE FIXATIVE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Cytocorp, Inc.. It received FDA 510(k) clearance on 1988-04-01 under 510(k) number K880549. The device is classified under product code LDY. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIACYTE FIXATIVE SOLUTION?

DIACYTE FIXATIVE SOLUTION is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Cytocorp, Inc.. The 510(k) number is K880549.

When did DIACYTE FIXATIVE SOLUTION receive FDA 510(k) clearance?

DIACYTE FIXATIVE SOLUTION received FDA 510(k) clearance on 1988-04-01, under 510(k) number K880549.

Who is the listed applicant for DIACYTE FIXATIVE SOLUTION?

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

What is the FDA product code for DIACYTE FIXATIVE SOLUTION?

The FDA product code for DIACYTE FIXATIVE SOLUTION is LDY.

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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.