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FDA 510(k)

CADWELL 7400

K-Number: K822214 · 1982-09-24

ApplicantCadwell Laboratories, Inc.
Decision Date1982-09-24
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CADWELL 7400 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 1982-09-24 under 510(k) number K822214. 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 7400?

CADWELL 7400 is a medical device that received FDA 510(k) clearance on 1982-09-24. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K822214.

When did CADWELL 7400 receive FDA 510(k) clearance?

CADWELL 7400 received FDA 510(k) clearance on 1982-09-24, under 510(k) number K822214.

Who is the listed applicant for CADWELL 7400?

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 7400?

The FDA product code for CADWELL 7400 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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