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FDA 510(k)

CADWELL EXCEL

K-Number: K880088 · 1988-05-04

ApplicantCadwell Laboratories, Inc.
Decision Date1988-05-04
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CADWELL EXCEL is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1988-05-04 under 510(k) number K880088. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADWELL EXCEL?

CADWELL EXCEL is a medical device that received FDA 510(k) clearance on 1988-05-04. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K880088.

When did CADWELL EXCEL receive FDA 510(k) clearance?

CADWELL EXCEL received FDA 510(k) clearance on 1988-05-04, under 510(k) number K880088.

Who is the listed applicant for CADWELL EXCEL?

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

What is the FDA product code for CADWELL EXCEL?

The FDA product code for CADWELL EXCEL is GWF.

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Other records listing Cadwell 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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