FDA 510(k)

DISPOSABLE ICP KIT DIFF. SIZES

K-Number: K840003 · 1984-02-28

Decision Date1984-02-28

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ICP KIT DIFF. SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1984-02-28 under 510(k) number K840003. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ICP KIT DIFF. SIZES?

DISPOSABLE ICP KIT DIFF. SIZES is a medical device that received FDA 510(k) clearance on 1984-02-28. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K840003.

When did DISPOSABLE ICP KIT DIFF. SIZES receive FDA 510(k) clearance?

DISPOSABLE ICP KIT DIFF. SIZES received FDA 510(k) clearance on 1984-02-28, under 510(k) number K840003.

Who is the listed applicant for DISPOSABLE ICP KIT DIFF. SIZES?

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

What is the FDA product code for DISPOSABLE ICP KIT DIFF. SIZES?

The FDA product code for DISPOSABLE ICP KIT DIFF. SIZES is GWM.

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Related Devices (Code: GWM)

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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.