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FDA 510(k)

EPIDURAL TRAYS

K-Number: K842095 · 1984-07-03

ApplicantConcord Laboratories, Inc.
Decision Date1984-07-03
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPIDURAL TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K842095. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPIDURAL TRAYS?

EPIDURAL TRAYS is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K842095.

When did EPIDURAL TRAYS receive FDA 510(k) clearance?

EPIDURAL TRAYS received FDA 510(k) clearance on 1984-07-03, under 510(k) number K842095.

Who is the listed applicant for EPIDURAL TRAYS?

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

What is the FDA product code for EPIDURAL TRAYS?

The FDA product code for EPIDURAL TRAYS is CAZ.

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Other records listing Concord Laboratories, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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