FDA 510(k)

EASYNET BODY POSITION MODULE

K-Number: K040932 · 2004-07-01

Decision Date2004-07-01

Product CodeLEL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EASYNET BODY POSITION MODULE 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 2004-07-01 under 510(k) number K040932. The device is classified under product code LEL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYNET BODY POSITION MODULE?

EASYNET BODY POSITION MODULE is a medical device that received FDA 510(k) clearance on 2004-07-01. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K040932.

When did EASYNET BODY POSITION MODULE receive FDA 510(k) clearance?

EASYNET BODY POSITION MODULE received FDA 510(k) clearance on 2004-07-01, under 510(k) number K040932.

Who is the listed applicant for EASYNET BODY POSITION MODULE?

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 EASYNET BODY POSITION MODULE?

The FDA product code for EASYNET BODY POSITION MODULE is LEL.

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Other records listing Cadwell Laboratories, Inc. as applicant

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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.