FDA 510(k)

CADWELL 6200 A

K-Number: K931428 · 1993-06-22

Decision Date1993-06-22

Product CodeGWF

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CADWELL 6200 A 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 1993-06-22 under 510(k) number K931428. 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 6200 A?

CADWELL 6200 A is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K931428.

When did CADWELL 6200 A receive FDA 510(k) clearance?

CADWELL 6200 A received FDA 510(k) clearance on 1993-06-22, under 510(k) number K931428.

Who is the listed applicant for CADWELL 6200 A?

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 6200 A?

The FDA product code for CADWELL 6200 A 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.