FDA 510(k)

C-POST

K-Number: K945370 · 1995-03-31

Decision Date1995-03-31

Product CodeELR

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

C-POST is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K945370. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-POST?

C-POST is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is Bisco, Inc.. The 510(k) number is K945370.

When did C-POST receive FDA 510(k) clearance?

C-POST received FDA 510(k) clearance on 1995-03-31, under 510(k) number K945370.

Who is the listed applicant for C-POST?

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

What is the FDA product code for C-POST?

The FDA product code for C-POST is ELR.

Other records listing Bisco, Inc. as applicant

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Related Devices (Code: ELR)

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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.