FDA 510(k)

A O HISTOSTAT EMBEDDING CTR #8030,32,34

K-Number: K821831 · 1982-07-13

Decision Date1982-07-13

Product CodeIDS

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

A O HISTOSTAT EMBEDDING CTR #8030,32,34 is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-07-13 under 510(k) number K821831. The device is classified under product code IDS. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A O HISTOSTAT EMBEDDING CTR #8030,32,34?

A O HISTOSTAT EMBEDDING CTR #8030,32,34 is a medical device that received FDA 510(k) clearance on 1982-07-13. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821831.

When did A O HISTOSTAT EMBEDDING CTR #8030,32,34 receive FDA 510(k) clearance?

A O HISTOSTAT EMBEDDING CTR #8030,32,34 received FDA 510(k) clearance on 1982-07-13, under 510(k) number K821831.

Who is the listed applicant for A O HISTOSTAT EMBEDDING CTR #8030,32,34?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A O HISTOSTAT EMBEDDING CTR #8030,32,34?

The FDA product code for A O HISTOSTAT EMBEDDING CTR #8030,32,34 is IDS.

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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.