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FDA 510(k)

SPLATTER SHIELD

K-Number: K915676 · 1992-09-11

ApplicantChathamborough Research Group, Inc.
Decision Date1992-09-11
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPLATTER SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Chathamborough Research Group, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K915676. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLATTER SHIELD?

SPLATTER SHIELD is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Chathamborough Research Group, Inc.. The 510(k) number is K915676.

When did SPLATTER SHIELD receive FDA 510(k) clearance?

SPLATTER SHIELD received FDA 510(k) clearance on 1992-09-11, under 510(k) number K915676.

Who is the listed applicant for SPLATTER SHIELD?

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

What is the FDA product code for SPLATTER SHIELD?

The FDA product code for SPLATTER SHIELD is FMF.

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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.

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